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dbVar

Database of genomic structural variation

nsv6131079

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:nsv5554765 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: 143 SVs from 28 studies. See in: genome view

Remapped(Score: Perfect):66,641,176-66,641,227

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131079	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	66,641,176	66,641,227
nsv6131079	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	64,637,294	64,637,345

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17958151	line1 insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17958151	Remapped	Perfect	NC_000017.11:g.666 41176_66641227ins?	GRCh38.p12	First Pass	NC_000017.11	Chr17	66,641,176	66,641,227
nssv17958151	Submitted genomic		NC_000017.10:g.646 37294_64637345ins?	GRCh37 (hg19)		NC_000017.10	Chr17	64,637,294	64,637,345

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)
nssv17958151	0.09	552	6130

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