A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528733



Internal ID15456026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:531504..792438hg38UCSC Ensembl
Innerchr10:577444..838378hg19UCSC Ensembl
Innerchr10:567444..828378hg18UCSC Ensembl
Innerchr10:567444..828378hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38260935
hg19260935
hg18260935
hg17260935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705389
Samples
Known GenesDIP2C, MIR5699, PRR26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528733
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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