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dbVar

Database of genomic structural variation

nsv5910497

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:79

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: 199 SVs from 35 studies. See in: genome view

Submitted genomic86,805,900-86,805,978

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5910497	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	86,805,900	86,805,978
nsv5910497	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	88,565,657	88,565,735

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17368538	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17368538	Submitted genomic		NC_000010.11:g.868 05900_86805978del	GRCh38 (hg38)		NC_000010.11	Chr10	86,805,900	86,805,978
nssv17368538	Remapped	Perfect	NC_000010.10:g.885 65657_88565735del	GRCh37.p13	First Pass	NC_000010.10	Chr10	88,565,657	88,565,735

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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