A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765293



Internal ID20541153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152182564..152182564hg38UCSC Ensembl
chrX:151351036..151351036hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289915
Samples
Known GenesGABRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765293
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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