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dbVar

Database of genomic structural variation

nsv5959542

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: 93 SVs from 18 studies. See in: genome view

Submitted genomic95,731,781-95,731,781

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5959542	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	95,731,781	95,731,781
nsv5959542	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	97,491,538	97,491,538

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17369252	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17369252	Submitted genomic		NC_000010.11:g.957 31781_95731782ins1 42	GRCh38 (hg38)		NC_000010.11	Chr10	95,731,781	95,731,781
nssv17369252	Remapped	Perfect	NC_000010.10:g.974 91538_97491539ins1 42	GRCh37.p13	First Pass	NC_000010.10	Chr10	97,491,538	97,491,538

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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