A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796220



Internal ID19166952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102288382..102358497hg38UCSC Ensembl
Innerchr9:105050664..105120779hg19UCSC Ensembl
Innerchr9:104090485..104160600hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3870116
hg1970116
hg1870116
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891699
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796220
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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