A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891524



Internal ID19185920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2681397..2699606hg38UCSC Ensembl
Outerchr9:2681397..2699606hg38UCSC Ensembl
Innerchr9:2681397..2699606hg19UCSC Ensembl
Outerchr9:2681397..2699606hg19UCSC Ensembl
Innerchr9:2671397..2689606hg18UCSC Ensembl
Outerchr9:2671397..2689606hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3818210
hg1918210
hg1818210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799028, essv25781171, essv25786050
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891524
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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