A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891687



Internal ID19186083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81181252..81214149hg38UCSC Ensembl
Outerchr9:81181252..81214149hg38UCSC Ensembl
Innerchr9:83796167..83829064hg19UCSC Ensembl
Outerchr9:83796167..83829064hg19UCSC Ensembl
Innerchr9:82985987..83018884hg18UCSC Ensembl
Outerchr9:82985987..83018884hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3832898
hg1932898
hg1832898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780527
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891687
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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