A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937429



Internal ID15884699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4012707..4099344hg38UCSC Ensembl
Innerchr20:3993354..4079991hg19UCSC Ensembl
Innerchr20:3941354..4027991hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3886638
hg1986638
hg1886638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585308
Supporting Variants
Samples
Known GenesRNF24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv937429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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