A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1997n54



Internal ID22769892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70136867..70142028hg38UCSC Ensembl
chr11:69982973..69988134hg19UCSC Ensembl
chr11:69660621..69665782hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385162
hg195162
hg185162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555355, nsv555346, nsv555371, nsv555369, nsv555364
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1997n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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