A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891586



Internal ID19185982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11676507..11963439hg38UCSC Ensembl
Outerchr9:11676507..11982510hg38UCSC Ensembl
Innerchr9:11676507..11963439hg19UCSC Ensembl
Outerchr9:11676507..11982510hg19UCSC Ensembl
Innerchr9:11666507..11953439hg18UCSC Ensembl
Outerchr9:11666507..11972510hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38306004
hg19306004
hg18306004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779360, essv25779389
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891586
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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