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dbVar

Database of genomic structural variation

nsv6308329

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:mobile element deletion
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:7,342

Description:nsv6147430 from Byrska-Bishop et. al 2021. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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: 180 SVs from 42 studies. See in: genome view

Remapped(Score: Perfect):76,042,708-76,050,049

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6308329	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	76,042,708	76,050,049
nsv6308329	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	76,963,861	76,971,202

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17664483	mobile element deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17664483	Remapped	Perfect	NC_000004.12:g.760 42708_76050049del	GRCh38.p12	First Pass	NC_000004.12	Chr4	76,042,708	76,050,049
nssv17664483	Submitted genomic		NC_000004.11:g.769 63861_76971202del	GRCh37 (hg19)		NC_000004.11	Chr4	76,963,861	76,971,202

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17664483	0.061	386	6376

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