A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525381



Internal ID301543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29806894..29806974hg38UCSC Ensembl
chr16:29818215..29818295hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707630
Samples
Known GenesMAZ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525381
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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