A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893109



Internal ID19183929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60040758..60053166hg38UCSC Ensembl
Outerchr18:60040758..60053166hg38UCSC Ensembl
Innerchr18:57707990..57720398hg19UCSC Ensembl
Outerchr18:57707990..57720398hg19UCSC Ensembl
Innerchr18:55858970..55871378hg18UCSC Ensembl
Outerchr18:55858970..55871378hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3812409
hg1912409
hg1812409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800182
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893109
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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