A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517361



Internal ID293787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66015975..66016064hg38UCSC Ensembl
chr16:66049878..66049967hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517361
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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