A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139666



Internal ID338855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:242126047..242178047hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3852001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv298n206
Supporting Variantsnssv16927217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139666
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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