A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3101n54



Internal ID22770996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31954821..31964446hg38UCSC Ensembl
chr13:32528958..32538583hg19UCSC Ensembl
chr13:31426958..31436583hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg389626
hg199626
hg189626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561402, nsv561404, nsv561403
Samples
Known GenesEEF1DP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3101n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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