A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893150



Internal ID19183970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73955809..73966933hg38UCSC Ensembl
Outerchr18:73955809..73966933hg38UCSC Ensembl
Innerchr18:71623044..71634168hg19UCSC Ensembl
Outerchr18:71623044..71634168hg19UCSC Ensembl
Innerchr18:69774024..69785148hg18UCSC Ensembl
Outerchr18:69774024..69785148hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3811125
hg1911125
hg1811125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781185
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893150
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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