A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377347



Internal ID22312529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2863418..2869501hg38UCSC Ensembl
chr16:2913419..2919502hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386084
hg196084
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197482
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14377347
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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