A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782429



Internal ID19166775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73302299..73388734hg38UCSC Ensembl
Innerchr18:70969534..71055969hg19UCSC Ensembl
Innerchr18:69120514..69206949hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3886436
hg1986436
hg1886436
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893146
Supporting Variants
Samples
Known GenesLOC100505817
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782429
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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