A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528787



Internal ID15109394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120586553..120722450hg38UCSC Ensembl
Innerchr10:122346065..122481962hg19UCSC Ensembl
Innerchr10:122336055..122471952hg18UCSC Ensembl
Innerchr10:122336055..122471952hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38135898
hg19135898
hg18135898
hg17135898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705457
Samples
Known GenesC10orf85, MIR5694, PPAPDC1A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528787
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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