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dbVar

Database of genomic structural variation

nsv5569845

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:155,154

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: 2139 SVs from 94 studies. See in: genome view

Submitted genomic39,374,555-39,529,708

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5569845	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	39,374,555	39,529,708
nsv5569845	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	39,232,074	39,387,227

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17158437	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
nssv17158437	Submitted genomic		NC_000008.11:g.393 74555_39529708delG	GRCh38 (hg38)		NC_000008.11	Chr8	39,374,555	39,529,708
nssv17158437	Remapped	Perfect	NC_000008.10:g.392 32074_39387227delG	GRCh37.p13	First Pass	NC_000008.10	Chr8	39,232,074	39,387,227

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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