A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3190n54



Internal ID22771085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63395129..63434791hg38UCSC Ensembl
chr13:63969262..64008924hg19UCSC Ensembl
chr13:62867263..62906925hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3839663
hg1939663
hg1839663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561903, nsv561905, nsv561904, nsv561906, nsv561902
Samples1780854536_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3190n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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