A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9228n54



Internal ID22777123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114408176..114517952hg38UCSC Ensembl
chr4:115329332..115439108hg19UCSC Ensembl
chr4:115548781..115658557hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38109777
hg19109777
hg18109777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595204, nsv595205
SamplesHGDP00579, HGDP00645, HGDP00641
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9228n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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