A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603022



Internal ID21551683
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 StatusM
Merged Variants
Supporting Variantsnssv17081789
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603022
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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