A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9782n54



Internal ID22777677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51981695..52131895hg38UCSC Ensembl
chr5:51277529..51427729hg19UCSC Ensembl
chr5:51313286..51463486hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38150201
hg19150201
hg18150201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598150, nsv598149
Samples1782681169_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9782n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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