A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2759410



Internal ID17833260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13332875..13358701hg38UCSC Ensembl
Innerchr16:13426732..13452558hg19UCSC Ensembl
Innerchr16:13334233..13360059hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3825827
hg1925827
hg1825827
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv978323
Supporting Variants
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2759410
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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