A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892432



Internal ID18836566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96058284..96367788hg38UCSC Ensembl
Outerchr13:96058284..96367788hg38UCSC Ensembl
Innerchr13:96710538..97020042hg19UCSC Ensembl
Outerchr13:96710538..97020042hg19UCSC Ensembl
Innerchr13:95508539..95818043hg18UCSC Ensembl
Outerchr13:95508539..95818043hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38309505
hg19309505
hg18309505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25793175
Samples
Known GenesHS6ST3
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892432
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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