A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv935231



Internal ID15882501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:592392..625245hg38UCSC Ensembl
Innerchr20:573036..605889hg19UCSC Ensembl
Innerchr20:521036..553889hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3832854
hg1932854
hg1832854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585173
Supporting Variants
Samples
Known GenesTCF15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv935231
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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