A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779389



Internal ID19177252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11676507..11963439hg38UCSC Ensembl
Innerchr9:11676507..11963439hg19UCSC Ensembl
Innerchr9:11666507..11953439hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38286933
hg19286933
hg18286933
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891586
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=85
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779389
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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