A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524477



Internal ID15105084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81325862..81328529hg38UCSC Ensembl
Innerchr16:81359467..81362134hg19UCSC Ensembl
Innerchr16:79916968..79919635hg18UCSC Ensembl
Innerchr16:79916968..79919635hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382668
hg192668
hg182668
hg172668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700415
Samples
Known GenesGAN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524477
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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