A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058665



Internal ID21967898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190059771..190059771hg38UCSC Ensembl
chr2:190924497..190924497hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535184
Samples
Known GenesMSTN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058665
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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