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dbVar

Database of genomic structural variation

nsv5915086

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:106

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: 369 SVs from 54 studies. See in: genome view

Submitted genomic17,875,482-17,875,587

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5915086	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	17,875,482	17,875,587
nsv5915086	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	17,732,991	17,733,096

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17439265	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17439265	Submitted genomic		NC_000008.11:g.178 75482_17875587del	GRCh38 (hg38)		NC_000008.11	Chr8	17,875,482	17,875,587
nssv17439265	Remapped	Perfect	NC_000008.10:g.177 32991_17733096del	GRCh37.p13	First Pass	NC_000008.10	Chr8	17,732,991	17,733,096

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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