A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041421



Internal ID21950756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171278882..171278882hg38UCSC Ensembl
chr2:172135392..172135392hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041421
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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