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dbVar

Database of genomic structural variation

nsv4726775

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:nsv4684718 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: 88 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):71,563,062-71,563,062

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4726775	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	71,563,062	71,563,062
nsv4726775	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	71,274,108	71,274,108

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16252711	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16252711	Remapped	Perfect	NC_000011.10:g.715 63062_71563063ins?	GRCh38.p12	First Pass	NC_000011.10	Chr11	71,563,062	71,563,062
nssv16252711	Submitted genomic		NC_000011.9:g.7127 4108_71274109ins?	GRCh37 (hg19)		NC_000011.9	Chr11	71,274,108	71,274,108

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)
nssv16252711	1	4552	4552

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