A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520378



Internal ID15447671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24265267..24394011hg38UCSC Ensembl
Innerchr10:24554196..24682940hg19UCSC Ensembl
Innerchr10:24594202..24722946hg18UCSC Ensembl
Innerchr10:24594202..24722946hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38128745
hg19128745
hg18128745
hg17128745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697381
Samples
Known GenesKIAA1217, MIR603
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520378
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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