A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697810



Internal ID15434462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76288033..76288610hg38UCSC Ensembl
Innerchr9:78902949..78903526hg19UCSC Ensembl
Innerchr9:78092769..78093346hg18UCSC Ensembl
Innerchr9:76132503..76133080hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38578
hg19578
hg18578
hg17578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521139
Supporting Variants
Samples
Known GenesPCSK5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697810
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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