A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3287n54



Internal ID22771182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83523737..83598939hg38UCSC Ensembl
chr13:84097872..84173074hg19UCSC Ensembl
chr13:82995873..83071075hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3875203
hg1975203
hg1875203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562535, nsv562519, nsv562518, nsv562537, nsv562521, nsv562533, nsv562534, nsv562538, nsv562536
SamplesHGDP01005, HGDP00860, HGDP00970, HGDP01049, HGDP00707, HGDP01046, HGDP01058, HGDP00793, HGDP00864, HGDP01057, HGDP00855, HGDP01044, HGDP00859
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3287n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss259
Observed Complex0
Frequencyn/a


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