A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055802



Internal ID21965035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120566369..120566369hg38UCSC Ensembl
chrX:119700224..119700224hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639160
Samples
Known GenesCUL4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055802
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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