A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536502



Internal ID311969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57981433..57981440hg38UCSC Ensembl
chr16:58015337..58015344hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709496
Samples
Known GenesTEPP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536502
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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