A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785434



Internal ID18814201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3989971..4029467hg38UCSC Ensembl
Innerchr3:4031655..4071151hg19UCSC Ensembl
Innerchr3:4006655..4046151hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3839497
hg1939497
hg1839497
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893633
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785434
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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