A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056010



Internal ID21965243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42447083..42447083hg38UCSC Ensembl
chr2:42674223..42674223hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519295
Samples
Known GenesKCNG3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056010
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer