A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893112



Internal ID19183932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:61573018..61579183hg38UCSC Ensembl
Outerchr18:61573018..61579183hg38UCSC Ensembl
Innerchr18:59240251..59246416hg19UCSC Ensembl
Outerchr18:59240251..59246416hg19UCSC Ensembl
Innerchr18:57391231..57397396hg18UCSC Ensembl
Outerchr18:57391231..57397396hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg386166
hg196166
hg186166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781509
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893112
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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