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dbVar

Database of genomic structural variation

nsv6308647

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:7,904

Description:nsv6147148 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: 80 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):29,992,070-29,999,973

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6308647	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	29,992,070	29,999,973
nsv6308647	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	30,033,561	30,041,464

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17661319	mobile element deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17661319	Remapped	Perfect	NC_000003.12:g.299 92070_29999973del	GRCh38.p12	First Pass	NC_000003.12	Chr3	29,992,070	29,999,973
nssv17661319	Submitted genomic		NC_000003.11:g.300 33561_30041464del	GRCh37 (hg19)		NC_000003.11	Chr3	30,033,561	30,041,464

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)
nssv17661319	0.013	83	6404

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