A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199090



Internal ID22348724
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14326059, nssv14326060
SamplesNA19239, NA19240
Known GenesCASC15
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199090
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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