A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638588



Internal ID21830635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:111721090..111721155hg38UCSC Ensembl
chrX:110964318..110964383hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107175
Supporting Variants
Samples
Known GenesALG13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638588
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