A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5548477



Internal ID322224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15832373..15832421hg38UCSC Ensembl
chr16:15926230..15926278hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705022
Samples
Known GenesMYH11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5548477
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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