A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525489



Internal ID15106096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65252967..65305991hg38UCSC Ensembl
Innerchr16:65286870..65339894hg19UCSC Ensembl
Innerchr16:63844371..63897395hg18UCSC Ensembl
Innerchr16:63844371..63897395hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3853025
hg1953025
hg1853025
hg1753025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701620
Samples
Known GenesLINC00922
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525489
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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