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dbVar

Database of genomic structural variation

nsv4769058

Organism: Homo sapiens

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

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

Description:nsv4685298 from Lee et. al 2020. 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: 113 SVs from 20 studies. See in: genome view

Remapped(Score: Perfect):93,876,103-93,876,103

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4769058	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	93,876,103	93,876,103
nsv4769058	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	94,341,659	94,341,659

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16252814	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16252814	Remapped	Perfect	NC_000001.11:g.938 76103_93876104ins?	GRCh38.p12	First Pass	NC_000001.11	Chr1	93,876,103	93,876,103
nssv16252814	Submitted genomic		NC_000001.10:g.943 41659_94341660ins?	GRCh37 (hg19)		NC_000001.10	Chr1	94,341,659	94,341,659

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)
nssv16252814	0.686	2860	4172

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