A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893117



Internal ID19183937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:65630436..65686399hg38UCSC Ensembl
Outerchr18:65630436..65686399hg38UCSC Ensembl
Innerchr18:63297672..63353635hg19UCSC Ensembl
Outerchr18:63297672..63353635hg19UCSC Ensembl
Innerchr18:61448652..61504615hg18UCSC Ensembl
Outerchr18:61448652..61504615hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3855964
hg1955964
hg1855964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785064
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893117
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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