nsv4378165

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:86
Validation:Not tested
Clinical Assertions: No
Region Size:104,532

Publication(s):Zarrei et al. 2019

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 1690 SVs from 93 studies. See in: genome view

Remapped(Score: Perfect):68,570,171-68,674,702

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4378165	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nsv4378165	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	69,435,889	69,540,420

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15612033	copy number gain	1-0642-003	SNP array	Genotyping	19
nssv15612426	copy number loss	1-0669-003	SNP array	Genotyping	24
nssv15612640	copy number gain	1-0704-003	SNP array	Genotyping	22
nssv15612801	copy number gain	1-0667-003	SNP array	Genotyping	20
nssv15614370	copy number gain	1-0745-003	SNP array	Genotyping	21
nssv15614591	copy number gain	1-0732-003	SNP array	Genotyping	21
nssv15616063	copy number gain	1-0781-003	SNP array	Genotyping	18
nssv15616745	copy number gain	1-0800-003	SNP array	Genotyping	26
nssv15617202	copy number gain	1-0814-003	SNP array	Genotyping	22
nssv15620286	copy number gain	1-0960-003	SNP array	Genotyping	23
nssv15620694	copy number gain	1-0992-003	SNP array	Genotyping	20
nssv15621856	copy number gain	1-1040-003	SNP array	Genotyping	20
nssv15621977	copy number gain	1-1001-003	SNP array	Genotyping	29
nssv15625485	copy number gain	1-0051-004	SNP array	Genotyping	21
nssv15625860	copy number gain	1-0389-005	SNP array	Genotyping	16
nssv15626072	copy number gain	1-0412-003	SNP array	Genotyping	28
nssv15626577	copy number gain	1-0446-006	SNP array	Genotyping	29
nssv15627703	copy number gain	1-0534-001	SNP array	Genotyping	23
nssv15629044	copy number gain	1-0548-001	SNP array	Genotyping	20
nssv15629406	copy number gain	1-0081-003	SNP array	Genotyping	16
nssv15629627	copy number gain	1-0583-003	SNP array	Genotyping	23
nssv15633356	copy number gain	12-4058-004	SNP array	Genotyping	29
nssv15633400	copy number gain	12-4098-002	SNP array	Genotyping	22
nssv15634593	copy number gain	12-4264-005	SNP array	Genotyping	21
nssv15635259	copy number gain	12-4139-003	SNP array	Genotyping	27
nssv15636234	copy number gain	14-0020-001	SNP array	Genotyping	22
nssv15636510	copy number gain	13-0078-002	SNP array	Genotyping	27
nssv15637076	copy number gain	14-0044-002	SNP array	Genotyping	25
nssv15637237	copy number gain	12-8115-001	SNP array	Genotyping	18
nssv15637254	copy number gain	12-8115-002	SNP array	Genotyping	18
nssv15641096	copy number gain	14-0382-004	SNP array	Genotyping	29
nssv15641396	copy number gain	14-0349-001	SNP array	Genotyping	23
nssv15641791	copy number gain	14-0276-001	SNP array	Genotyping	18
nssv15642087	copy number gain	15-1130-002	SNP array	Genotyping	17
nssv15642212	copy number gain	16-1002-002	SNP array	Genotyping	21
nssv15642588	copy number gain	15-1132-003	SNP array	Genotyping	21
nssv15642857	copy number gain	15-1111-001	SNP array	Genotyping	18
nssv15642877	copy number gain	15-1111-002	SNP array	Genotyping	20
nssv15643128	copy number gain	14-0326-001	SNP array	Genotyping	15
nssv15643233	copy number gain	14-0362-001	SNP array	Genotyping	18
nssv15644326	copy number gain	16-1006-001	SNP array	Genotyping	24
nssv15645598	copy number gain	16-1018-004	SNP array	Genotyping	22
nssv15646373	copy number gain	2-1182-002	SNP array	Genotyping	18
nssv15646509	copy number gain	2-1189-003	SNP array	Genotyping	24
nssv15647959	copy number gain	2-1314-004	SNP array	Genotyping	15
nssv15648662	copy number gain	2-1280-002	SNP array	Genotyping	19
nssv15649778	copy number gain	2-1352-003	SNP array	Genotyping	26
nssv15650941	copy number gain	2-1427-003	SNP array	Genotyping	19
nssv15652353	copy number gain	2-1502-003	SNP array	Genotyping	17
nssv15654490	copy number gain	2-1644-004	SNP array	Genotyping	28
nssv15656104	copy number gain	3-0657-000	SNP array	Genotyping	16
nssv15656208	copy number gain	3-0708-000	SNP array	Genotyping	21
nssv15656275	copy number gain	3-0719-001	SNP array	Genotyping	16
nssv15657626	copy number gain	4-0039-002	SNP array	Genotyping	25
nssv15660507	copy number gain	5-0003-004	SNP array	Genotyping	16
nssv15661262	copy number gain	5-0066-001	SNP array	Genotyping	23
nssv15661882	copy number loss	4-0043-001	SNP array	Genotyping	18
nssv15661967	copy number loss	5-0071-001	SNP array	Genotyping	26
nssv15662969	copy number gain	215795S	SNP array	Genotyping	24
nssv15663770	copy number loss	5-0124-003	SNP array	Genotyping	21
nssv15664780	copy number loss	5-0015-004	SNP array	Genotyping	13
nssv15665967	copy number loss	5-0025-003	SNP array	Genotyping	27
nssv15668404	copy number gain	7-0203-003	SNP array	Genotyping	15
nssv15670648	copy number gain	7-0200-003	SNP array	Genotyping	24
nssv15672609	copy number loss	9-0011-002	SNP array	Genotyping	18
nssv15672990	copy number gain	9-0019-002	SNP array	Genotyping	27
nssv15674262	copy number loss	9-0025-001	SNP array	Genotyping	23
nssv15676849	copy number gain	181071	SNP array	Genotyping	24
nssv15677619	copy number gain	215808	SNP array	Genotyping	29
nssv15678344	copy number gain	191455	SNP array	Genotyping	23
nssv15678581	copy number gain	162335	SNP array	Genotyping	19
nssv15679209	copy number loss	184228	SNP array	Genotyping	23
nssv15679992	copy number gain	229188S	SNP array	Genotyping	30
nssv15680196	copy number gain	222685	SNP array	Genotyping	22
nssv15680577	copy number gain	214098	SNP array	Genotyping	20
nssv15681318	copy number gain	232508	SNP array	Genotyping	15
nssv15685152	copy number gain	OCD165-8961163	SNP array	Genotyping	21
nssv15688004	copy number loss	192222	SNP array	Genotyping	19
nssv15691877	copy number loss	OCD80-896843	SNP array	Genotyping	27
nssv15692319	copy number loss	OCD55-0625-9391-1	SNP array	Genotyping	23
nssv15695413	copy number gain	187888	SNP array	Genotyping	17
nssv15698793	copy number gain	239647	SNP array	Genotyping	15
nssv15698822	copy number gain	178077	SNP array	Genotyping	17
nssv15699030	copy number gain	188858	SNP array	Genotyping	23
nssv15699088	copy number gain	196900	SNP array	Genotyping	18
nssv15699860	copy number loss	170722	SNP array	Genotyping	24

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15612033	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15612426	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15612640	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15612801	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15614370	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15614591	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15616063	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15616745	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15617202	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15620286	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15620694	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15621856	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15621977	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15625485	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15625860	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15626072	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15626577	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15627703	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15629044	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15629406	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15629627	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15633356	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15633400	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15634593	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15635259	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15636234	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15636510	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15637076	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15637237	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15637254	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15641096	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15641396	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15641791	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15642087	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15642212	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15642588	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15642857	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15642877	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15643128	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15643233	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15644326	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15645598	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15646373	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15646509	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15647959	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15648662	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15649778	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15650941	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15652353	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15654490	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15656104	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15656208	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15656275	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15657626	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15660507	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15661262	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15661882	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15661967	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15662969	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15663770	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15664780	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15665967	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15668404	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15670648	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15672609	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15672990	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15674262	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15676849	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15677619	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15678344	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15678581	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15679209	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15679992	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15680196	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15680577	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15681318	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15685152	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15688004	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15691877	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15692319	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15695413	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15698793	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15698822	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15699030	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15699088	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15699860	Remapped	Perfect	NC_000004.12:g.(?_ 68570171)_(6867470 2_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	68,570,171	68,674,702
nssv15612033	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15612426	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15612640	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15612801	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15614370	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15614591	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15616063	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15616745	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15617202	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15620286	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15620694	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15621856	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15621977	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420
nssv15625485	Submitted genomic		NC_000004.11:g.(?_ 69435889)_(6954042 0_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	69,435,889	69,540,420

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dbVar

Database of genomic structural variation

nsv4378165

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant