A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613199



Internal ID16400608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5385783..5407628hg38UCSC Ensembl
Innerchr9:5385783..5407628hg19UCSC Ensembl
Innerchr9:5375783..5397628hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3821846
hg1921846
hg1821846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12487n54
Supporting Variantsnssv1156219
SamplesHGDP00993
Known GenesPLGRKT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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