A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892413



Internal ID19183233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86906887..87156170hg38UCSC Ensembl
Outerchr13:86906887..87156170hg38UCSC Ensembl
Innerchr13:87559142..87808425hg19UCSC Ensembl
Outerchr13:87559142..87808425hg19UCSC Ensembl
Innerchr13:86357143..86606426hg18UCSC Ensembl
Outerchr13:86357143..86606426hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38249284
hg19249284
hg18249284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792629
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892413
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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