A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5548754



Internal ID322479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9477747..9477749hg38UCSC Ensembl
chr16:9571604..9571606hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5548754
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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