A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221418



Internal ID22365814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11637965..11638056hg38UCSC Ensembl
chr16:11731821..11731912hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14389535, nssv14388423
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221418
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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