A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585175



Internal ID16372584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:602943..614136hg38UCSC Ensembl
Innerchr20:583587..594780hg19UCSC Ensembl
Innerchr20:531587..542780hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3811194
hg1911194
hg1811194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7421n54
Supporting Variantsnssv935232
Samples
Known GenesTCF15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585175
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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