A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526574



Internal ID15453867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55050833..55056999hg38UCSC Ensembl
Innerchr16:55084745..55090911hg19UCSC Ensembl
Innerchr16:53642246..53648412hg18UCSC Ensembl
Innerchr16:53642246..53648412hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg386167
hg196167
hg186167
hg176167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702891
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526574
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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