A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025889



Internal ID84998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65569061..65580161hg38UCSC Ensembl
chr9:44845889..44856994hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3811101
hg1911106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025889
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02259


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