A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527696



Internal ID15454989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:20936183..20971754hg38UCSC Ensembl
Innerchr6:20936414..20971985hg19UCSC Ensembl
Innerchr6:21044393..21079964hg18UCSC Ensembl
Innerchr6:21044393..21079964hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3835572
hg1935572
hg1835572
hg1735572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704174
Samples
Known GenesCDKAL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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