A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800599



Internal ID19167979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37938391..37944758hg38UCSC Ensembl
Innerchr3:37979882..37986249hg19UCSC Ensembl
Innerchr3:37954886..37961253hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg386368
hg196368
hg186368
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893682
Supporting Variants
Samples
Known GenesCTDSPL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800599
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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