A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891641



Internal ID19186037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24467700..24491589hg38UCSC Ensembl
Outerchr9:24457293..24495243hg38UCSC Ensembl
Innerchr9:24467698..24491587hg19UCSC Ensembl
Outerchr9:24457291..24495241hg19UCSC Ensembl
Innerchr9:24457698..24481587hg18UCSC Ensembl
Outerchr9:24447291..24485241hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3837951
hg1937951
hg1837951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792420, essv25789975, essv25789998
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891641
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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