A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891676



Internal ID19186072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41539712..41679418hg38UCSC Ensembl
Outerchr9:41539712..41679418hg38UCSC Ensembl
Innerchr9:46008981..46148687hg19UCSC Ensembl
Outerchr9:46008981..46148687hg19UCSC Ensembl
Innerchr9:45898977..46038683hg18UCSC Ensembl
Outerchr9:45898977..46038683hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38139707
hg19139707
hg18139707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792888
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891676
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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