A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024315



Internal ID83948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72369024..72380229hg38UCSC Ensembl
chr9:74983940..74995145hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3811206
hg1911206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024315
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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