A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3263n54



Internal ID22771158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77697665..77698337hg38UCSC Ensembl
chr13:78271800..78272472hg19UCSC Ensembl
chr13:77169801..77170473hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38673
hg19673
hg18673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562383, nsv562384
Samples
Known GenesMIR3665, SLAIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3263n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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