A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891712



Internal ID18839422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112900188..113053118hg38UCSC Ensembl
Outerchr9:112900188..113053118hg38UCSC Ensembl
Innerchr9:115662468..115815398hg19UCSC Ensembl
Outerchr9:115662468..115815398hg19UCSC Ensembl
Innerchr9:114702289..114855219hg18UCSC Ensembl
Outerchr9:114702289..114855219hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38152931
hg19152931
hg18152931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787654
Samples
Known GenesZFP37, ZNF883
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891712
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer