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dbVar

Database of genomic structural variation

nsv6115277

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:52

Description:nsv5416608 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: 116 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):45,042,897-45,042,948

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6115277	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	45,042,897	45,042,948
nsv6115277	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000020.10	Chr20	43,671,538	43,671,589

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17966572	alu insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17966572	Remapped	Perfect	NC_000020.11:g.450 42897_45042948ins?	GRCh38.p12	First Pass	NC_000020.11	Chr20	45,042,897	45,042,948
nssv17966572	Submitted genomic		NC_000020.10:g.436 71538_43671589ins?	GRCh37 (hg19)		NC_000020.10	Chr20	43,671,538	43,671,589

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)
nssv17966572	0.034	217	6404

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