A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526781



Internal ID15107388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176880503..176889200hg38UCSC Ensembl
Innerchr5:176307504..176316201hg19UCSC Ensembl
Innerchr5:176240110..176248807hg18UCSC Ensembl
Innerchr5:176240110..176248807hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg388698
hg198698
hg188698
hg178698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv362n21
Supporting Variantsnssv703133
Samples
Known GenesHK3, UNC5A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526781
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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