A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045956



Internal ID21955208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16225124..16225124hg38UCSC Ensembl
chr2:16406392..16406392hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045956
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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