A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786848



Internal ID18833879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6650885..6703997hg38UCSC Ensembl
Innerchr9:6650885..6703997hg19UCSC Ensembl
Innerchr9:6640885..6693997hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3853113
hg1953113
hg1853113
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891541
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786848
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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