A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv995937



Internal ID16289893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39707188..39710252hg38UCSC Ensembl
Innerchr4:39708808..39711872hg19UCSC Ensembl
Innerchr4:39385203..39388267hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg383065
hg193065
hg183065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594014
Supporting Variants
Samples
Known GenesUBE2K
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv995937
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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