A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1992n54



Internal ID22769887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70132159..70137956hg38UCSC Ensembl
chr11:69978265..69984062hg19UCSC Ensembl
chr11:69655913..69661710hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385798
hg195798
hg185798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555335, nsv555333, nsv555331, nsv555332, nsv555334
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1992n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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