A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891552



Internal ID19185948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8087483..8117656hg38UCSC Ensembl
Outerchr9:8087483..8117656hg38UCSC Ensembl
Innerchr9:8087483..8117656hg19UCSC Ensembl
Outerchr9:8087483..8117656hg19UCSC Ensembl
Innerchr9:8077483..8107656hg18UCSC Ensembl
Outerchr9:8077483..8107656hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3830174
hg1930174
hg1830174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786097
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891552
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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