A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388338



Internal ID22243172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31254481..31254792hg38UCSC Ensembl
chr16:31265802..31266113hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224702
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14388338
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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