A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141086



Internal ID340281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67339474..67339624hg38UCSC Ensembl
chr5:66635302..66635452hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16966660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141086
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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