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dbVar

Database of genomic structural variation

nsv4369922

Organism: Homo sapiens

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

Variant Calls:3
Validation:Not tested
Clinical Assertions: No
Region Size:36,589

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: 334 SVs from 43 studies. See in: genome view

Remapped(Score: Perfect):94,187,074-94,223,662

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4369922	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	94,187,074	94,223,662
nsv4369922	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	95,199,302	95,235,890

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15640645	copy number gain	14-0349-003	SNP array	Genotyping	20
nssv15641401	copy number gain	14-0349-001	SNP array	Genotyping	23
nssv15641438	copy number gain	14-0349-004	SNP array	Genotyping	21

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15640645	Remapped	Perfect	NC_000008.11:g.(?_ 94187074)_(9422366 2_?)dup	GRCh38.p12	First Pass	NC_000008.11	Chr8	94,187,074	94,223,662
nssv15641401	Remapped	Perfect	NC_000008.11:g.(?_ 94187074)_(9422366 2_?)dup	GRCh38.p12	First Pass	NC_000008.11	Chr8	94,187,074	94,223,662
nssv15641438	Remapped	Perfect	NC_000008.11:g.(?_ 94187074)_(9422366 2_?)dup	GRCh38.p12	First Pass	NC_000008.11	Chr8	94,187,074	94,223,662
nssv15640645	Submitted genomic		NC_000008.10:g.(?_ 95199302)_(9523589 0_?)dup	GRCh37 (hg19)		NC_000008.10	Chr8	95,199,302	95,235,890
nssv15641401	Submitted genomic		NC_000008.10:g.(?_ 95199302)_(9523589 0_?)dup	GRCh37 (hg19)		NC_000008.10	Chr8	95,199,302	95,235,890
nssv15641438	Submitted genomic		NC_000008.10:g.(?_ 95199302)_(9523589 0_?)dup	GRCh37 (hg19)		NC_000008.10	Chr8	95,199,302	95,235,890

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

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