A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218877



Internal ID22364085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67956628..67957053hg38UCSC Ensembl
chr16:67990531..67990956hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14386055, nssv14379779, nssv14380318, nssv14392436
SamplesNA19238, NA19239, HG00731, HG00732
Known GenesSLC12A4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218877
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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