A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8926n54



Internal ID20142350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3403438..3449382hg38UCSC Ensembl
chr4:3405165..3451109hg19UCSC Ensembl
chr4:3374963..3420907hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3845945
hg1945945
hg1845945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593452, nsv593451, nsv593450
SamplesHGDP01191, HGDP00975, HGDP00330
Known GenesHGFAC, RGS12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8926n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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