nsv4374470

Organism: Homo sapiens

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

Variant Calls:50
Validation:Not tested
Clinical Assertions: No
Region Size:75,534

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: 941 SVs from 79 studies. See in: genome view

Remapped(Score: Perfect):1,905,134-1,980,667

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4374470	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nsv4374470	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000018.9	Chr18	1,905,135	1,980,668

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15611604	copy number loss	1-0649-003	SNP array	Genotyping	17
nssv15617777	copy number loss	1-0850-004	SNP array	Genotyping	17
nssv15620634	copy number loss	1-0976-003	SNP array	Genotyping	17
nssv15620655	copy number loss	1-0976-004	SNP array	Genotyping	21
nssv15621458	copy number loss	1-1017-003	SNP array	Genotyping	20
nssv15622327	copy number loss	1-1028-003	SNP array	Genotyping	22
nssv15625731	copy number loss	1-0346-001	SNP array	Genotyping	24
nssv15631945	copy number loss	1-1061-003	SNP array	Genotyping	19
nssv15634834	copy number loss	12-8214-001	SNP array	Genotyping	20
nssv15634863	copy number loss	12-8214-003	SNP array	Genotyping	24
nssv15637515	copy number loss	14-0050-001	SNP array	Genotyping	14
nssv15637531	copy number loss	14-0050-002	SNP array	Genotyping	20
nssv15639034	copy number loss	14-0246-001	SNP array	Genotyping	22
nssv15639054	copy number loss	14-0246-002	SNP array	Genotyping	22
nssv15649444	copy number loss	2-1401-003	SNP array	Genotyping	30
nssv15650003	copy number loss	2-1425-001	SNP array	Genotyping	27
nssv15650422	copy number loss	2-1480-001	SNP array	Genotyping	18
nssv15650918	copy number loss	2-1425-004	SNP array	Genotyping	20
nssv15651142	copy number loss	2-1425-003	SNP array	Genotyping	20
nssv15652244	copy number loss	2-1550-002	SNP array	Genotyping	24
nssv15657247	copy number loss	3-0321-000	SNP array	Genotyping	27
nssv15657383	copy number loss	3-0490-000	SNP array	Genotyping	24
nssv15660274	copy number loss	3-0719-000	SNP array	Genotyping	19
nssv15660292	copy number loss	3-0719-001	SNP array	Genotyping	16
nssv15663665	copy number loss	5-1008-003	SNP array	Genotyping	10
nssv15665874	copy number loss	7-0100-004	SNP array	Genotyping	19
nssv15669252	copy number loss	7-0168-003	SNP array	Genotyping	21
nssv15671257	copy number loss	7-0280-001	SNP array	Genotyping	22
nssv15671297	copy number loss	7-0280-004	SNP array	Genotyping	17
nssv15671314	copy number loss	7-0280-005	SNP array	Genotyping	18
nssv15671363	copy number loss	7-0280-008	SNP array	Genotyping	21
nssv15675552	copy number loss	169695	SNP array	Genotyping	14
nssv15677845	copy number loss	218115	SNP array	Genotyping	26
nssv15680596	copy number loss	215105	SNP array	Genotyping	32
nssv15680853	copy number loss	232715S	SNP array	Genotyping	25
nssv15682169	copy number loss	219367	SNP array	Genotyping	17
nssv15682949	copy number loss	OCD120-B_1732	SNP array	Genotyping	28
nssv15683068	copy number loss	238146S	SNP array	Genotyping	16
nssv15683242	copy number loss	OCD1007-S_0625-5706-3	SNP array	Genotyping	19
nssv15683519	copy number loss	OCD125-896992	SNP array	Genotyping	24
nssv15683541	copy number loss	OCD125-896993	SNP array	Genotyping	28
nssv15687875	copy number loss	OCD51-S_0625-7445-2	SNP array	Genotyping	16
nssv15689821	copy number loss	OCD1150-S_HAM473	SNP array	Genotyping	24
nssv15691604	copy number loss	OCD57-0625-9923-1	SNP array	Genotyping	18
nssv15696067	copy number loss	155362	SNP array	Genotyping	22
nssv15696847	copy number loss	218093	SNP array	Genotyping	20
nssv15698016	copy number loss	198587	SNP array	Genotyping	22
nssv15698037	copy number loss	200039	SNP array	Genotyping	25
nssv15699958	copy number loss	209017	SNP array	Genotyping	23
nssv15700359	copy number loss	201955	SNP array	Genotyping	21

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15611604	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15617777	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15620634	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15620655	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15621458	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15622327	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15625731	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15631945	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15634834	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15634863	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15637515	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15637531	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15639034	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15639054	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15649444	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15650003	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15650422	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15650918	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15651142	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15652244	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15657247	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15657383	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15660274	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15660292	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15663665	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15665874	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15669252	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15671257	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15671297	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15671314	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15671363	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15675552	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15677845	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15680596	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15680853	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15682169	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15682949	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15683068	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15683242	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15683519	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15683541	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15687875	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15689821	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15691604	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15696067	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15696847	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15698016	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15698037	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15699958	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15700359	Remapped	Perfect	NC_000018.10:g.(?_ 1905134)_(1980667_ ?)del	GRCh38.p12	First Pass	NC_000018.10	Chr18	1,905,134	1,980,667
nssv15611604	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15617777	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15620634	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15620655	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15621458	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15622327	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15625731	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15631945	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15634834	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15634863	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15637515	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15637531	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15639034	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15639054	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15649444	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15650003	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15650422	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15650918	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15651142	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15652244	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15657247	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15657383	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15660274	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15660292	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15663665	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15665874	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15669252	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15671257	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15671297	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15671314	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15671363	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15675552	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15677845	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15680596	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15680853	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15682169	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15682949	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15683068	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15683242	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15683519	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15683541	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15687875	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15689821	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15691604	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15696067	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15696847	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15698016	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15698037	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15699958	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668
nssv15700359	Submitted genomic		NC_000018.9:g.(?_1 905135)_(1980668_? )del	GRCh37 (hg19)		NC_000018.9	Chr18	1,905,135	1,980,668

dbVar

Database of genomic structural variation

nsv4374470

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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