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dbVar

Database of genomic structural variation

nsv6626412

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:88,579

Publication(s):Zarrei et al. 2023

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: 564 SVs from 68 studies. See in: genome view

Remapped(Score: Perfect):9,258,342-9,346,920

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6626412	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	9,258,342	9,346,920
nsv6626412	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	9,318,401	9,406,979

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18314672	duplication	OSC0824	SNP array	Probe signal intensity	7
nssv18321397	duplication	OSC1101	SNP array	Probe signal intensity	6

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18314672	Remapped	Perfect	NC_000001.11:g.(?_ 9258342)_(9346920_ ?)dup	GRCh38.p12	First Pass	NC_000001.11	Chr1	9,258,342	9,346,920
nssv18321397	Remapped	Perfect	NC_000001.11:g.(?_ 9258342)_(9346920_ ?)dup	GRCh38.p12	First Pass	NC_000001.11	Chr1	9,258,342	9,346,920
nssv18314672	Submitted genomic		NC_000001.10:g.(?_ 9318401)_(9406979_ ?)dup	GRCh37 (hg19)		NC_000001.10	Chr1	9,318,401	9,406,979
nssv18321397	Submitted genomic		NC_000001.10:g.(?_ 9318401)_(9406979_ ?)dup	GRCh37 (hg19)		NC_000001.10	Chr1	9,318,401	9,406,979

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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