A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14383277



Internal ID22268004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2862684..2863031hg38UCSC Ensembl
chr16:2912685..2913032hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227901
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14383277
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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