A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022756



Internal ID82860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80200757..80204279hg38UCSC Ensembl
chr9:82815672..82819194hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg383523
hg193523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022756
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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