A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8910n54



Internal ID20142334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2249015..2262496hg38UCSC Ensembl
chr4:2250742..2264223hg19UCSC Ensembl
chr4:2220540..2234021hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3813482
hg1913482
hg1813482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593379, nsv593378, nsv593382, nsv593381, nsv593380
Samples
Known GenesMIR4800, MXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8910n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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