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dbVar

Database of genomic structural variation

nsv5973996

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: 333 SVs from 26 studies. See in: genome view

Submitted genomic132,670,032-132,670,032

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5973996	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	132,670,032	132,670,032
nsv5973996	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	134,483,536	134,483,536

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17355650	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17355650	Submitted genomic		NC_000010.11:g.132 670032_132670033in s60	GRCh38 (hg38)		NC_000010.11	Chr10	132,670,032	132,670,032
nssv17355650	Remapped	Perfect	NC_000010.10:g.134 483536_134483537in s60	GRCh37.p13	First Pass	NC_000010.10	Chr10	134,483,536	134,483,536

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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