A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3349n54



Internal ID20136773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98576248..98577597hg38UCSC Ensembl
chr13:99228502..99229851hg19UCSC Ensembl
chr13:98026503..98027852hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381350
hg191350
hg181350
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562889, nsv562894, nsv562886, nsv562888, nsv562882, nsv562887, nsv562893
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3349n54
Frequency
Sample Size17421
Observed Gain40
Observed Loss12
Observed Complex0
Frequencyn/a


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