A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081789



Internal ID21465226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13802014..13802079hg38UCSC Ensembl
chr16:13895871..13895936hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603022
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081789
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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