A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011105



Internal ID22072736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71336239..71376776hg38UCSC Ensembl
Outerchr15:71335630..71379761hg38UCSC Ensembl
Innerchr15:71628578..71669115hg19UCSC Ensembl
Outerchr15:71627969..71672100hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3844132
hg1944132
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155188
Supporting Variants
Samples
Known GenesTHSD4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011105
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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