A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024286



Internal ID83932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71986620..71990469hg38UCSC Ensembl
chr9:74601536..74605385hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383850
hg193850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024286
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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