A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782132



Internal ID19167621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:40381939..40403627hg38UCSC Ensembl
Innerchr3:40423430..40445118hg19UCSC Ensembl
Innerchr3:40398434..40420122hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3821689
hg1921689
hg1821689
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893685
Supporting Variants
Samples
Known GenesENTPD3, ENTPD3-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782132
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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