A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761954



Internal ID17528615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70148750..70164354hg38UCSC Ensembl
Innerchr16:70182653..70198257hg19UCSC Ensembl
Innerchr16:68740154..68755758hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3815605
hg1915605
hg1815605
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv960372
Supporting Variants
SamplesHGDP01284
Known GenesPDPR
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761954
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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