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dbVar

Database of genomic structural variation

nsv5584942

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:291

Publication(s):Ebert et al. 2021

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: 128 SVs from 24 studies. See in: genome view

Submitted genomic73,194,168-73,194,458

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5584942	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	73,194,168	73,194,458
nsv5584942	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	71,190,307	71,190,597

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17098560	deletion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17098560	Submitted genomic		NC_000017.11:g.731 94168_73194458delT	GRCh38 (hg38)		NC_000017.11	Chr17	73,194,168	73,194,458
nssv17098560	Remapped	Perfect	NC_000017.10:g.711 90307_71190597delT	GRCh37.p13	First Pass	NC_000017.10	Chr17	71,190,307	71,190,597

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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