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dbVar

Database of genomic structural variation

nsv5567699

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:7,777

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: 176 SVs from 38 studies. See in: genome view

Submitted genomic205,249,150-205,256,926

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5567699	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	205,249,150	205,256,926
nsv5567699	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	206,113,874	206,121,650

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17109961	deletion	SAMN00004622	Sequencing	Sequence alignment	1,208

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17109961	Submitted genomic		NC_000002.12:g.205 249150_205256926de lC	GRCh38 (hg38)		NC_000002.12	Chr2	205,249,150	205,256,926
nssv17109961	Remapped	Perfect	NC_000002.11:g.206 113874_206121650de lC	GRCh37.p13	First Pass	NC_000002.11	Chr2	206,113,874	206,121,650

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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