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dbVar

Database of genomic structural variation

nsv5909493

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:56

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

Submitted genomic98,393,369-98,393,424

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5909493	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	98,393,369	98,393,424
nsv5909493	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	101,155,651	101,155,706

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17448229	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17448229	Submitted genomic		NC_000009.12:g.983 93369_98393424del	GRCh38 (hg38)		NC_000009.12	Chr9	98,393,369	98,393,424
nssv17448229	Remapped	Perfect	NC_000009.11:g.101 155651_101155706de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	101,155,651	101,155,706

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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