A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978324



Internal ID18266843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:50325790..50328674hg38UCSC Ensembl
Innerchr16:50359701..50362585hg19UCSC Ensembl
Innerchr16:48917202..48920086hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg382885
hg192885
hg182885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762755
SamplesHGDP00456
Known GenesBRD7
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978324
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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