A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524799



Internal ID300989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81636960..81642432hg38UCSC Ensembl
chr16:81670565..81676037hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg385473
hg195473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709858
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524799
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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