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dbVar

Database of genomic structural variation

nsv6132922

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:33,061

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: 254 SVs from 49 studies. See in: genome view

Remapped(Score: Perfect):80,645,763-80,678,823

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv6132922	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	80,645,763	80,645,777	80,678,815	80,678,823
nsv6132922	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	80,679,660	80,679,674	80,712,712	80,712,720

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17683407	deletion	SAMN20524661	Sequencing	Paired-end mapping	62

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17683407	Remapped	Perfect	NC_000016.10:g.(80 645763_80645777)_( 80678815_80678823) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	80,645,763	80,645,777	80,678,815	80,678,823
nssv17683407	Submitted genomic		NC_000016.9:g.(806 79660_80679674)_(8 0712712_80712720)d el	GRCh37 (hg19)		NC_000016.9	Chr16	80,679,660	80,679,674	80,712,712	80,712,720

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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