A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155188



Internal ID22085693
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011105
Samples
Known GenesTHSD4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155188
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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