A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526694



Internal ID15453987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85961978..85963990hg38UCSC Ensembl
Innerchr16:85995584..85997596hg19UCSC Ensembl
Innerchr16:84553085..84555097hg18UCSC Ensembl
Innerchr16:84553085..84555097hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382013
hg192013
hg182013
hg172013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703031
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526694
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer