A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059913



Internal ID21969146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77834228..77834228hg38UCSC Ensembl
chrX:77089725..77089725hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644175
Samples
Known GenesMAGT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059913
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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