A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023090



Internal ID83104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63544264..63796000hg38UCSC Ensembl
chr9:68139998..68391734hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38251737
hg19251737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485372
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023090
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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