A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526856



Internal ID15454149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9527012..9529732hg38UCSC Ensembl
Innerchr16:9620869..9623589hg19UCSC Ensembl
Innerchr16:9528370..9531090hg18UCSC Ensembl
Innerchr16:9528370..9531090hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg382721
hg192721
hg182721
hg172721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703214
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526856
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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