A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3061n54



Internal ID22770956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18589694..18922294hg38UCSC Ensembl
chr13:19163834..19496434hg19UCSC Ensembl
chr13:18061834..18394434hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38332601
hg19332601
hg18332601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561153, nsv561154, nsv561155
Samples
Known GenesANKRD20A9P, LINC00408, LINC00417
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3061n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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