A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525433



Internal ID15452726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73473731..73541259hg38UCSC Ensembl
Innerchr15:73766072..73833600hg19UCSC Ensembl
Innerchr15:71553125..71620653hg18UCSC Ensembl
Innerchr15:71553125..71620653hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3867529
hg1967529
hg1867529
hg1767529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701560
Samples
Known GenesC15orf60
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525433
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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