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dbVar

Database of genomic structural variation

nsv6624926

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:129,210

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: 1931 SVs from 95 studies. See in: genome view

Remapped(Score: Perfect):42,739,025-42,868,234

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6624926	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	42,739,025	42,868,234
nsv6624926	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	43,243,177	43,372,386

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18283741	duplication	OSC2451	SNP array	Probe signal intensity	6
nssv18284801	duplication	OSC2547	SNP array	Probe signal intensity	9

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18283741	Remapped	Perfect	NC_000019.10:g.(?_ 42739025)_(4286823 4_?)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	42,739,025	42,868,234
nssv18284801	Remapped	Perfect	NC_000019.10:g.(?_ 42739025)_(4286823 4_?)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	42,739,025	42,868,234
nssv18283741	Submitted genomic		NC_000019.9:g.(?_4 3243177)_(43372386 _?)dup	GRCh37 (hg19)		NC_000019.9	Chr19	43,243,177	43,372,386
nssv18284801	Submitted genomic		NC_000019.9:g.(?_4 3243177)_(43372386 _?)dup	GRCh37 (hg19)		NC_000019.9	Chr19	43,243,177	43,372,386

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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