A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524913



Internal ID15452206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71332783..71376173hg38UCSC Ensembl
Innerchr15:71625122..71668512hg19UCSC Ensembl
Innerchr15:69412176..69455566hg18UCSC Ensembl
Innerchr15:69412176..69455566hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3843391
hg1943391
hg1843391
hg1743391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700925
Samples
Known GenesTHSD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524913
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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