A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613192



Internal ID16400601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5311171..5407628hg38UCSC Ensembl
Innerchr9:5311171..5407628hg19UCSC Ensembl
Innerchr9:5301171..5397628hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3896458
hg1996458
hg1896458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126524
Samples
Known GenesPLGRKT, RLN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613192
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