A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941618



Internal ID15888888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57525185..57526801hg38UCSC Ensembl
Innerchr20:56100241..56101857hg19UCSC Ensembl
Innerchr20:55533647..55535263hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381617
hg191617
hg181617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586316
Supporting Variants
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv941618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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