A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529520



Internal ID305535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50904209..50904849hg38UCSC Ensembl
chr16:50938120..50938760hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529520
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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