A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528338



Internal ID15455631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:50839084..50871099hg38UCSC Ensembl
Innerchr16:50872995..50905010hg19UCSC Ensembl
Innerchr16:49430496..49462511hg18UCSC Ensembl
Innerchr16:49430496..49462511hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3832016
hg1932016
hg1832016
hg1732016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704920
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528338
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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