A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519474



Internal ID15446767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:160902417..160912479hg38UCSC Ensembl
Innerchr3:160620205..160630267hg19UCSC Ensembl
Innerchr3:162102899..162112961hg18UCSC Ensembl
Innerchr3:162102907..162112969hg17UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3810063
hg1910063
hg1810063
hg1710063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696872
Samples
Known GenesPPM1L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519474
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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