A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520258



Internal ID15447551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71608889..71610479hg38UCSC Ensembl
Innerchr15:71901228..71902818hg19UCSC Ensembl
Innerchr15:69688282..69689872hg18UCSC Ensembl
Innerchr15:69688282..69689872hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381591
hg191591
hg181591
hg171591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662142, nssv685728
Samples
Known GenesTHSD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520258
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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