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dbVar

Database of genomic structural variation

nsv5912752

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:78

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: 300 SVs from 29 studies. See in: genome view

Submitted genomic131,172,242-131,172,319

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5912752	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	131,172,242	131,172,319
nsv5912752	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	132,970,505	132,970,582

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17358624	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17358624	Submitted genomic		NC_000010.11:g.131 172242_131172319de l	GRCh38 (hg38)		NC_000010.11	Chr10	131,172,242	131,172,319
nssv17358624	Remapped	Perfect	NC_000010.10:g.132 970505_132970582de l	GRCh37.p13	First Pass	NC_000010.10	Chr10	132,970,505	132,970,582

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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