A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892374



Internal ID19183194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65058204..65140650hg38UCSC Ensembl
Outerchr13:65058204..65148152hg38UCSC Ensembl
Innerchr13:65632336..65714782hg19UCSC Ensembl
Outerchr13:65632336..65722284hg19UCSC Ensembl
Innerchr13:64530337..64612783hg18UCSC Ensembl
Outerchr13:64530337..64620285hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3889949
hg1989949
hg1889949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798128, essv25800519, essv25797701
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892374
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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