A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289915



Internal ID20499133
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 StatusS
Merged Variantsnsv4765293
Supporting Variants
Samples
Known GenesGABRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289915
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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