A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023411



Internal ID83322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74701363..74711425hg38UCSC Ensembl
chr9:77316279..77326341hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810063
hg1910063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141428
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023411
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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