A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3388n54



Internal ID22771283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109782884..109787607hg38UCSC Ensembl
chr13:110435231..110439954hg19UCSC Ensembl
chr13:109233232..109237955hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384724
hg194724
hg184724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563091, nsv563089, nsv563090
Samples
Known GenesIRS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3388n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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