A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058487



Internal ID21967720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6533380..6533380hg38UCSC Ensembl
chrX:6451421..6451421hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648661
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058487
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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