A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892411



Internal ID19183231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86342553..86393572hg38UCSC Ensembl
Outerchr13:86297319..86408028hg38UCSC Ensembl
Innerchr13:86994808..87045827hg19UCSC Ensembl
Outerchr13:86949574..87060283hg19UCSC Ensembl
Innerchr13:85792809..85843828hg18UCSC Ensembl
Outerchr13:85747575..85858284hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38110710
hg19110710
hg18110710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799231, essv25782122, essv25779948
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892411
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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