A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150964



Internal ID15506803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63159264..63248817hg38UCSC Ensembl
Innerchr20:61790616..61880169hg19UCSC Ensembl
Innerchr20:61261061..61350614hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3889554
hg1989554
hg1889554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586558
Supporting Variants
Samples1780854231_A
Known GenesBIRC7, MIR124-3, MIR3196, NKAIN4, YTHDF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150964
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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