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dbVar

Database of genomic structural variation

nsv5568765

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:74

Publication(s):Ebert et al. 2021

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: 113 SVs from 31 studies. See in: genome view

Submitted genomic94,659,438-94,659,511

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5568765	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	94,659,438	94,659,511
nsv5568765	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	94,288,750	94,288,823

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17153331	deletion	SAMN00006466	Sequencing	Sequence alignment	4,625

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17153331	Submitted genomic		NC_000007.14:g.946 59438_94659511delG	GRCh38 (hg38)		NC_000007.14	Chr7	94,659,438	94,659,511
nssv17153331	Remapped	Perfect	NC_000007.13:g.942 88750_94288823delG	GRCh37.p13	First Pass	NC_000007.13	Chr7	94,288,750	94,288,823

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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