A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639351



Internal ID21831398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118278350..118278516hg38UCSC Ensembl
chrX:117412313..117412479hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639351
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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