A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892409



Internal ID19183229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84753612..85059443hg38UCSC Ensembl
Outerchr13:84753612..85059443hg38UCSC Ensembl
Innerchr13:85327747..85633578hg19UCSC Ensembl
Outerchr13:85327747..85633578hg19UCSC Ensembl
Innerchr13:84225748..84531579hg18UCSC Ensembl
Outerchr13:84225748..84531579hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38305832
hg19305832
hg18305832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791998
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892409
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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