A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528861



Internal ID304902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75231216..75232191hg38UCSC Ensembl
chr16:75265114..75266089hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710164
Samples
Known GenesBCAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528861
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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