A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639152



Internal ID21831199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41702030..41702442hg38UCSC Ensembl
chrX:41561283..41561695hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106615
Supporting Variants
Samples
Known GenesCASK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639152
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