A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009733



Internal ID74137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41775334..41776473hg38UCSC Ensembl
chr8:41632852..41633991hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484346
Supporting Variants
Samples
Known GenesANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001717


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