A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125843



Internal ID15979029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102645..272191hg38UCSC Ensembl
Innerchr9:102645..272191hg19UCSC Ensembl
Innerchr9:92645..262191hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38169547
hg19169547
hg18169547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612983
Supporting Variants
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125843
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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