A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786426



Internal ID18833528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:81648181..81679366hg38UCSC Ensembl
Innerchr3:81697332..81728517hg19UCSC Ensembl
Innerchr3:81780022..81811207hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3831186
hg1931186
hg1831186
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893729
Supporting Variants
Samples
Known GenesGBE1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786426
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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