A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206856



Internal ID22355338
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14332555
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206856
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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