A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326860



Internal ID22174196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26540813..26543279hg38UCSC Ensembl
chr6:26541041..26543507hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg382467
hg192467
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209127
Supporting Variants
SamplesHG00514
Known GenesHMGN4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326860
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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