A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520362



Internal ID15447655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60977046..60986023hg38UCSC Ensembl
Innerchr15:61269245..61278222hg19UCSC Ensembl
Innerchr15:59056537..59065514hg18UCSC Ensembl
Innerchr15:59056537..59065514hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg388978
hg198978
hg188978
hg178978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682198, nssv698504, nssv663239
Samples
Known GenesRORA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520362
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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