A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326059



Internal ID22274886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21672138..21672472hg38UCSC Ensembl
chr6:21672369..21672703hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199090
Supporting Variants
SamplesNA19239
Known GenesCASC15
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326059
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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