A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613181



Internal ID16053904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5267043..5335470hg38UCSC Ensembl
Innerchr9:5267043..5335470hg19UCSC Ensembl
Innerchr9:5257043..5325470hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3868428
hg1968428
hg1868428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126513
Samples
Known GenesRLN1, RLN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613181
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