A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14389089



Internal ID22196764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30839499..30840236hg38UCSC Ensembl
chr16:30850820..30851557hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3239177
Supporting Variants
SamplesHG00731
Known GenesBCL7C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14389089
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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