A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788518



Internal ID19173086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:161562..228301hg38UCSC Ensembl
Innerchr9:161562..228301hg19UCSC Ensembl
Innerchr9:151562..218301hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3866740
hg1966740
hg1866740
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891507
Supporting Variants
Samples
Known GenesC9orf66, CBWD1, DOCK8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788518
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