A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332555



Internal ID22144045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170029658..170030109hg38UCSC Ensembl
chr6:170344882..170345333hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206856
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332555
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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