A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525265



Internal ID15105872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75377738..75399962hg38UCSC Ensembl
Innerchr15:75670079..75692303hg19UCSC Ensembl
Innerchr15:73457132..73479356hg18UCSC Ensembl
Innerchr15:73457132..73479356hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3822225
hg1922225
hg1822225
hg1722225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701365
Samples
Known GenesSIN3A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525265
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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