A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141665



Internal ID340862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138262950..138268500hg38UCSC Ensembl
chr11:144048..149569hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg385551
hg195522
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141665
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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