A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702053



Internal ID125719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75157146..75211143hg38UCSC Ensembl
chr15:75449487..75503484hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3853998
hg1953998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527235
Supporting Variants
Samples
Known GenesC15orf39
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702053
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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