A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024329



Internal ID83957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72408680..72411141hg38UCSC Ensembl
chr9:75023596..75026057hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382462
hg192462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024329
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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