A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784547



Internal ID19173455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16383440..16391296hg38UCSC Ensembl
Innerchr9:16383438..16391294hg19UCSC Ensembl
Innerchr9:16373438..16381294hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg387857
hg197857
hg187857
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891622
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784547
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