A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797853



Internal ID19177781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72609740..72669862hg38UCSC Ensembl
Innerchr1:73075423..73135545hg19UCSC Ensembl
Innerchr1:72848011..72908133hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3860123
hg1960123
hg1860123
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893701
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797853
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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