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dbVar

Database of genomic structural variation

nsv5980340

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: 110 SVs from 32 studies. See in: genome view

Submitted genomic24,741,973-24,741,973

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5980340	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	24,741,973	24,741,973
nsv5980340	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	24,763,519	24,763,519

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17357068	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17357068	Submitted genomic		NC_000011.10:g.247 41973_24741974ins8 1	GRCh38 (hg38)		NC_000011.10	Chr11	24,741,973	24,741,973
nssv17357068	Remapped	Perfect	NC_000011.9:g.2476 3519_24763520ins81	GRCh37.p13	First Pass	NC_000011.9	Chr11	24,763,519	24,763,519

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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