A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893146



Internal ID19183966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73302299..73388734hg38UCSC Ensembl
Outerchr18:73302299..73391387hg38UCSC Ensembl
Innerchr18:70969534..71055969hg19UCSC Ensembl
Outerchr18:70969534..71058622hg19UCSC Ensembl
Innerchr18:69120514..69206949hg18UCSC Ensembl
Outerchr18:69120514..69209602hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3889089
hg1989089
hg1889089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785948, essv25782429
Samples
Known GenesLOC100505817
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893146
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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