A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892294



Internal ID18836428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18636286..18942494hg38UCSC Ensembl
Outerchr13:18450119..19057038hg38UCSC Ensembl
Innerchr13:19210426..19516634hg19UCSC Ensembl
Outerchr13:19024259..19631178hg19UCSC Ensembl
Innerchr13:18108426..18414634hg18UCSC Ensembl
Outerchr13:17922259..18529178hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38606920
hg19606920
hg18606920
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781648, essv25791314, essv25791775
Samples
Known GenesANKRD20A9P, LINC00408, LINC00417, LINC00442
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892294
Frequency
Sample Size3017
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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