A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523867



Internal ID15451160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:94307465..94453604hg38UCSC Ensembl
Innerchr5:93643170..93789309hg19UCSC Ensembl
Innerchr5:93668926..93815065hg18UCSC Ensembl
Innerchr5:93668926..93815065hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38146140
hg19146140
hg18146140
hg17146140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv347n21
Supporting Variantsnssv699705
Samples
Known GenesKIAA0825
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523867
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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