A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586132



Internal ID16026855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45785138..45842587hg38UCSC Ensembl
Innerchr20:44413777..44471226hg19UCSC Ensembl
Innerchr20:43847184..43904633hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3857450
hg1957450
hg1857450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940870
Samples
Known GenesACOT8, DNTTIP1, SNX21, TNNC2, UBE2C, WFDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586132
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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