A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027634



Internal ID86127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112894330..112902220hg38UCSC Ensembl
chr9:115656610..115664500hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg387891
hg197891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490168
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027634
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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