A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1963n54



Internal ID20135387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64174262..64329761hg38UCSC Ensembl
chr11:63941734..64097233hg19UCSC Ensembl
chr11:63698310..63853809hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38155500
hg19155500
hg18155500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555186, nsv555185
Samples1780862275_A
Known GenesBAD, DNAJC4, ESRRA, FERMT3, FKBP2, GPR137, KCNK4, NUDT22, PLCB3, PPP1R14B, PRDX5, STIP1, TEX40, TRMT112, TRPT1, VEGFB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1963n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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