A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542341



Internal ID316769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24612466..24612468hg38UCSC Ensembl
chr16:24623787..24623789hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542341
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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