A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126530



Internal ID15979716
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 StatusS
Merged Variantsnsv613201
Supporting Variants
Samples
Known GenesPLGRKT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126530
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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