A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800758



Internal ID19160211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90290567..90390153hg38UCSC Ensembl
Innerchr3:90339717..90439303hg19UCSC Ensembl
Innerchr3:90422407..90521993hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3899587
hg1999587
hg1899587
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893740
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800758
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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