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dbVar

Database of genomic structural variation

nsv5968943

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: 80 SVs from 22 studies. See in: genome view

Submitted genomic72,596,475-72,596,475

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5968943	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	72,596,475	72,596,475
nsv5968943	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	72,307,519	72,307,519

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17356383	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17356383	Submitted genomic		NC_000011.10:g.725 96475_72596476ins2 06	GRCh38 (hg38)		NC_000011.10	Chr11	72,596,475	72,596,475
nssv17356383	Remapped	Perfect	NC_000011.9:g.7230 7519_72307520ins20 6	GRCh37.p13	First Pass	NC_000011.9	Chr11	72,307,519	72,307,519

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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