A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1982n54



Internal ID18994158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67605006..67666398hg38UCSC Ensembl
chr11:67372477..67433869hg19UCSC Ensembl
chr11:67129053..67190445hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3861393
hg1961393
hg1861393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555271, nsv555270
Samples1780862003_A, 1780862484_A
Known GenesACY3, ALDH3B2, DOC2GP, NDUFV1, NUDT8, TBX10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1982n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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