A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022868



Internal ID82940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38035741..38039421hg38UCSC Ensembl
chr9:38035738..38039418hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg383681
hg193681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478779
Supporting Variants
Samples
Known GenesSHB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022868
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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