A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613201



Internal ID16400610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5386384..5412546hg38UCSC Ensembl
Innerchr9:5386384..5412546hg19UCSC Ensembl
Innerchr9:5376384..5402546hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3826163
hg1926163
hg1826163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12487n54
Supporting Variantsnssv1126530
Samples
Known GenesPLGRKT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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