A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535856



Internal ID311438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45001615..45001666hg38UCSC Ensembl
chr21:46421530..46421581hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727186
Samples
Known GenesLINC00162
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535856
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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