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dbVar

Database of genomic structural variation

nsv6292597

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:11

Description:nsv5412847 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: 125 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):161,019,993-161,020,003

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6292597	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	161,019,993	161,020,003
nsv6292597	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	160,989,783	160,989,793

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17674787	alu insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17674787	Remapped	Perfect	NC_000001.11:g.161 019993_161020003in s?	GRCh38.p12	First Pass	NC_000001.11	Chr1	161,019,993	161,020,003
nssv17674787	Submitted genomic		NC_000001.10:g.160 989783_160989793in s?	GRCh37 (hg19)		NC_000001.10	Chr1	160,989,783	160,989,793

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)
nssv17674787	0.254	1443	5688

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