A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978323



Internal ID18613528
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759410
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978323
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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