A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529007



Internal ID15456300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60945201..60976083hg38UCSC Ensembl
Innerchr15:61237400..61268282hg19UCSC Ensembl
Innerchr15:59024692..59055574hg18UCSC Ensembl
Innerchr15:59024692..59055574hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3830883
hg1930883
hg1830883
hg1730883
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705717
Samples
Known GenesRORA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529007
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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