A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521665



Internal ID15448958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:133306110..133307099hg38UCSC Ensembl
Innerchr6:133627248..133628237hg19UCSC Ensembl
Innerchr6:133668941..133669930hg18UCSC Ensembl
Innerchr6:133668941..133669930hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38990
hg19990
hg18990
hg17990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698284
Samples
Known GenesEYA4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521665
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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