A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3093n54



Internal ID20136517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24700388..24756889hg38UCSC Ensembl
chr13:25274526..25331027hg19UCSC Ensembl
chr13:24172526..24229027hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3856502
hg1956502
hg1856502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561350, nsv561349
Samples
Known GenesATP12A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3093n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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