A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615854



Internal ID16403263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135257320..135414214hg38UCSC Ensembl
Innerchr9:138149166..138306060hg19UCSC Ensembl
Innerchr9:137288987..137445881hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38156895
hg19156895
hg18156895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12979n54
Supporting Variantsnssv1146798, nssv1146797
Samples
Known GenesC9orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615854
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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