A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9024n54



Internal ID22776919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42695536..42710097hg38UCSC Ensembl
chr4:42697553..42712114hg19UCSC Ensembl
chr4:42392310..42406871hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3814562
hg1914562
hg1814562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594056, nsv594057, nsv594059, nsv594058, nsv594060, nsv594061
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9024n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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