A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215129



Internal ID22361564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14288135..14288713hg38UCSC Ensembl
chr16:14381992..14382570hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377097, nssv14381718
SamplesNA19239, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215129
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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