A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3330n54



Internal ID20136754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96090080..96090978hg38UCSC Ensembl
chr13:96742334..96743232hg19UCSC Ensembl
chr13:95540335..95541233hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562791, nsv562786, nsv562789, nsv562790
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3330n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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