A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892342



Internal ID19183162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49799448..49811120hg38UCSC Ensembl
Outerchr13:49799448..49811120hg38UCSC Ensembl
Innerchr13:50373584..50385256hg19UCSC Ensembl
Outerchr13:50373584..50385256hg19UCSC Ensembl
Innerchr13:49271585..49283257hg18UCSC Ensembl
Outerchr13:49271585..49283257hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3811673
hg1911673
hg1811673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781731
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892342
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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