A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613699



Internal ID16054422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17470128..17490561hg38UCSC Ensembl
Innerchr9:17470126..17490559hg19UCSC Ensembl
Innerchr9:17460126..17480559hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3820434
hg1920434
hg1820434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1129327
Samples
Known GenesCNTLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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