A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326056



Internal ID22267175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21551551..21554650hg38UCSC Ensembl
chr6:21551782..21554881hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199970
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326056
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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