A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294885



Internal ID20504103
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 StatusS
Merged Variantsnsv4746029
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294885
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer