A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645535



Internal ID21837582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49291330..49291330hg38UCSC Ensembl
chrX:49147798..49147798hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054499
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645535
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