A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14375752



Internal ID22295791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15591986..15591986hg38UCSC Ensembl
chr16:15685843..15685843hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3548666
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14375752
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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