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dbVar

Database of genomic structural variation

nsv5576476

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:204

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

Submitted genomic190,101,191-190,101,394

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5576476	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	190,101,191	190,101,394
nsv5576476	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	189,818,980	189,819,183

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17131468	deletion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17131468	Submitted genomic		NC_000003.12:g.190 101191_190101394de lA	GRCh38 (hg38)		NC_000003.12	Chr3	190,101,191	190,101,394
nssv17131468	Remapped	Perfect	NC_000003.11:g.189 818980_189819183de lA	GRCh37.p13	First Pass	NC_000003.11	Chr3	189,818,980	189,819,183

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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