A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522374



Internal ID15449667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52186030..52194833hg38UCSC Ensembl
Innerchr16:52219942..52228745hg19UCSC Ensembl
Innerchr16:50777443..50786246hg18UCSC Ensembl
Innerchr16:50777443..50786246hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg388804
hg198804
hg188804
hg178804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695153
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522374
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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