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dbVar

Database of genomic structural variation

nsv5965883

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

Links to Other Resources

Overlapping Genes

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: 802 SVs from 65 studies. See in: genome view

Submitted genomic168,078,608-168,078,608

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5965883	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	168,078,608	168,078,608
nsv5965883	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	168,479,288	168,479,288

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17421241	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17421241	Submitted genomic		NC_000006.12:g.168 078608_168078609in s54	GRCh38 (hg38)		NC_000006.12	Chr6	168,078,608	168,078,608
nssv17421241	Remapped	Perfect	NC_000006.11:g.168 479288_168479289in s54	GRCh37.p13	First Pass	NC_000006.11	Chr6	168,479,288	168,479,288

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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