A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585265



Internal ID16372674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2634462..2641352hg38UCSC Ensembl
Innerchr20:2615108..2621998hg19UCSC Ensembl
Innerchr20:2563108..2569998hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386891
hg196891
hg186891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937305
Samples
Known GenesTMC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585265
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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