A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139469



Internal ID338655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32068158..32072327hg38UCSC Ensembl
chr2:32293227..32297396hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg384170
hg194170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16911376
Samples
Known GenesSPAST
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139469
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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