A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3329n54



Internal ID20136753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96090029..96090868hg38UCSC Ensembl
chr13:96742283..96743122hg19UCSC Ensembl
chr13:95540284..95541123hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38840
hg19840
hg18840
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562784, nsv562783, nsv562787
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3329n54
Frequency
Sample Size17421
Observed Gain8
Observed Loss6
Observed Complex0
Frequencyn/a


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