A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055268



Internal ID21964501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210337267..210337267hg38UCSC Ensembl
chr2:211201991..211201991hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055268
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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