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dbVar

Database of genomic structural variation

nsv6295010

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:nsv5403281 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: 125 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):85,467,267-85,467,318

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6295010	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	85,467,267	85,467,318
nsv6295010	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	85,096,583	85,096,634

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17650139	alu insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17650139	Remapped	Perfect	NC_000007.14:g.854 67267_85467318ins?	GRCh38.p12	First Pass	NC_000007.14	Chr7	85,467,267	85,467,318
nssv17650139	Submitted genomic		NC_000007.13:g.850 96583_85096634ins?	GRCh37 (hg19)		NC_000007.13	Chr7	85,096,583	85,096,634

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)
nssv17650139	0.127	802	6310

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