A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385857



Internal ID22238911
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236054
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385857
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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