A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746029



Internal ID20522040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80193742..80193742hg38UCSC Ensembl
chrX:79449241..79449241hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746029
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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