A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3444n54



Internal ID22771339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113378974..113400011hg38UCSC Ensembl
chr13:114033289..114054326hg19UCSC Ensembl
chr13:113081290..113102327hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3821038
hg1921038
hg1821038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563334, nsv563356
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3444n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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