A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156219



Internal ID15877444
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 StatusS
Merged Variantsnsv613199
Supporting Variants
SamplesHGDP00993
Known GenesPLGRKT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156219
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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