A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891699



Internal ID19186095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102288382..102358497hg38UCSC Ensembl
Outerchr9:102288382..102358497hg38UCSC Ensembl
Innerchr9:105050664..105120779hg19UCSC Ensembl
Outerchr9:105050664..105120779hg19UCSC Ensembl
Innerchr9:104090485..104160600hg18UCSC Ensembl
Outerchr9:104090485..104160600hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3870116
hg1970116
hg1870116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796220, essv25797840
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891699
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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