A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329472



Internal ID22256131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85158960..85159062hg38UCSC Ensembl
chr6:85868678..85868780hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527928
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329472
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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