A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3328n54



Internal ID20136752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96089978..96090868hg38UCSC Ensembl
chr13:96742232..96743122hg19UCSC Ensembl
chr13:95540233..95541123hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38891
hg19891
hg18891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562785, nsv562788, nsv562781
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3328n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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