A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137566



Internal ID15990752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76304935..76306933hg38UCSC Ensembl
Innerchr9:78919851..78921849hg19UCSC Ensembl
Innerchr9:78109671..78111669hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381999
hg191999
hg181999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614694
Supporting Variants
Samples
Known GenesPCSK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1137566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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