A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585179



Internal ID16372588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:609956..612997hg38UCSC Ensembl
Innerchr20:590600..593641hg19UCSC Ensembl
Innerchr20:538600..541641hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383042
hg193042
hg183042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv935235
Samples
Known GenesTCF15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585179
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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