A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8923n54



Internal ID20142347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3281695..3340410hg38UCSC Ensembl
chr4:3283422..3342137hg19UCSC Ensembl
chr4:3253220..3311935hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3858716
hg1958716
hg1858716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593440, nsv593441
Samples1780854479_A
Known GenesRGS12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8923n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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