A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700960



Internal ID15437612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3165103..3192615hg38UCSC Ensembl
Innerchr16:3215104..3242615hg19UCSC Ensembl
Innerchr16:3155105..3182616hg18UCSC Ensembl
Innerchr16:3155105..3182616hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3827513
hg1927512
hg1827512
hg1727512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524943
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700960
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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