A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523601



Internal ID15104208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72570840..72719890hg38UCSC Ensembl
Innerchr11:72281884..72430935hg19UCSC Ensembl
Innerchr11:71959532..72108583hg18UCSC Ensembl
Innerchr11:71959532..72108583hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38149051
hg19149052
hg18149052
hg17149052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699394
Samples
Known GenesARAP1, MIR139, PDE2A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523601
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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