A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796433



Internal ID19165758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:30226266..30299934hg38UCSC Ensembl
Innerchr3:30267757..30341425hg19UCSC Ensembl
Innerchr3:30242761..30316429hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3873669
hg1973669
hg1873669
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893680
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796433
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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