A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236054



Internal ID22373470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69182947..69185693hg38UCSC Ensembl
chr16:69216850..69219596hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382747
hg192747
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377306, nssv14385857
SamplesHG00512, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236054
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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