A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641779



Internal ID21833826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138970282..138970282hg38UCSC Ensembl
chrX:138052444..138052444hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046518
Supporting Variants
Samples
Known GenesFGF13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641779
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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