A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792671



Internal ID18816332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92163398..92538277hg38UCSC Ensembl
Innerchr9:94925680..95300559hg19UCSC Ensembl
Innerchr9:93965501..94340380hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38374880
hg19374880
hg18374880
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891693
Supporting Variants
Samples
Known GenesASPN, CENPP, ECM2, IARS, MIR3651, MIR4670, NOL8, OGN, OMD, SNORA84
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=34
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792671
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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