A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176390



Internal ID15856058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135258742..135414214hg38UCSC Ensembl
Innerchr9:138150588..138306060hg19UCSC Ensembl
Innerchr9:137290409..137445881hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38155473
hg19155473
hg18155473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615860
Supporting Variants
Samples1798860567_A
Known GenesC9orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176390
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