A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176387



Internal ID15855500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135247660..135414214hg38UCSC Ensembl
Innerchr9:138139506..138306060hg19UCSC Ensembl
Innerchr9:137279327..137445881hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38166555
hg19166555
hg18166555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615846
Supporting Variants
Samples1782681087_A
Known GenesC9orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176387
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