A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10012n54



Internal ID22777907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113740398..113848514hg38UCSC Ensembl
chr5:113076095..113184211hg19UCSC Ensembl
chr5:113103994..113212110hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38108117
hg19108117
hg18108117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599409, nsv599408
SamplesHGDP00991
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10012n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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