A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1738n54



Internal ID22769633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31373337..31375414hg38UCSC Ensembl
chr11:31394884..31396961hg19UCSC Ensembl
chr11:31351460..31353537hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382078
hg192078
hg182078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553977, nsv553978, nsv553975
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1738n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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