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dbVar

Database of genomic structural variation

nsv5901161

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:171

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: 116 SVs from 23 studies. See in: genome view

Submitted genomic134,615,529-134,615,699

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5901161	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	134,615,529	134,615,699
nsv5901161	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	134,334,371	134,334,541

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17404107	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17404107	Submitted genomic		NC_000003.12:g.134 615529_134615699de l	GRCh38 (hg38)		NC_000003.12	Chr3	134,615,529	134,615,699
nssv17404107	Remapped	Perfect	NC_000003.11:g.134 334371_134334541de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	134,334,371	134,334,541

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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