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dbVar

Database of genomic structural variation

nsv5576886

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:51

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: 134 SVs from 34 studies. See in: genome view

Submitted genomic27,101,385-27,101,435

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5576886	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	27,101,385	27,101,435
nsv5576886	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	27,324,253	27,324,303

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17112869	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
nssv17112869	Submitted genomic		NC_000002.12:g.271 01385_27101435delG	GRCh38 (hg38)		NC_000002.12	Chr2	27,101,385	27,101,435
nssv17112869	Remapped	Perfect	NC_000002.11:g.273 24253_27324303delG	GRCh37.p13	First Pass	NC_000002.11	Chr2	27,324,253	27,324,303

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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