A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796453



Internal ID18818516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129234668..129241234hg38UCSC Ensembl
Innerchr9:131996947..132003513hg19UCSC Ensembl
Innerchr9:131036768..131043334hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386567
hg196567
hg186567
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891728
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796453
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