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dbVar

Database of genomic structural variation

nsv6116921

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:nsv5428612 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: 132 SVs from 28 studies. See in: genome view

Remapped(Score: Perfect):78,195,482-78,195,533

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6116921	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	78,195,482	78,195,533
nsv6116921	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	78,487,824	78,487,875

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17964335	alu insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17964335	Remapped	Perfect	NC_000015.10:g.781 95482_78195533ins?	GRCh38.p12	First Pass	NC_000015.10	Chr15	78,195,482	78,195,533
nssv17964335	Submitted genomic		NC_000015.9:g.7848 7824_78487875ins?	GRCh37 (hg19)		NC_000015.9	Chr15	78,487,824	78,487,875

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)
nssv17964335	0.028	180	6404

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