A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9016n54



Internal ID22776911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39707188..39712123hg38UCSC Ensembl
chr4:39708808..39713743hg19UCSC Ensembl
chr4:39385203..39390138hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384936
hg194936
hg184936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594015, nsv594017, nsv594016, nsv594019, nsv594018
Samples
Known GenesUBE2K
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9016n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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