A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150941



Internal ID15854412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:380145..444790hg38UCSC Ensembl
Innerchr20:360789..425434hg19UCSC Ensembl
Innerchr20:308789..373434hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3864646
hg1964646
hg1864646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585171
Supporting Variants
Samples1780862101_A
Known GenesRBCK1, TBC1D20, TRIB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150941
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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