A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3259n54



Internal ID20136683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75635745..75636718hg38UCSC Ensembl
chr13:76209881..76210854hg19UCSC Ensembl
chr13:75107882..75108855hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38974
hg19974
hg18974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562356, nsv562358, nsv562352, nsv562357
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3259n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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