A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523103



Internal ID15450396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76288033..76289107hg38UCSC Ensembl
Innerchr9:78902949..78904023hg19UCSC Ensembl
Innerchr9:78092769..78093843hg18UCSC Ensembl
Innerchr9:76132503..76133577hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381075
hg191075
hg181075
hg171075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698799
Samples
Known GenesPCSK5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523103
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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