A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3258n54



Internal ID20136682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75635643..75636921hg38UCSC Ensembl
chr13:76209779..76211057hg19UCSC Ensembl
chr13:75107780..75109058hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg381279
hg191279
hg181279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562350, nsv562355, nsv562354
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3258n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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