A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787654



Internal ID18818448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112900188..113053118hg38UCSC Ensembl
Innerchr9:115662468..115815398hg19UCSC Ensembl
Innerchr9:114702289..114855219hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38152931
hg19152931
hg18152931
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891712
Supporting Variants
Samples
Known GenesZFP37, ZNF883
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=59
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787654
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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