A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051543



Internal ID21960776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190690012..190690012hg38UCSC Ensembl
chr2:191554738..191554738hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527804
Samples
Known GenesNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051543
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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