A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9783n54



Internal ID22777678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52037296..52146437hg38UCSC Ensembl
chr5:51333130..51442271hg19UCSC Ensembl
chr5:51368887..51478028hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38109142
hg19109142
hg18109142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598157, nsv598152, nsv598156, nsv598151, nsv598155, nsv598153, nsv598154
SamplesHGDP00925
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9783n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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