A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739671



Internal ID163337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23184652..23209586hg38UCSC Ensembl
chrX:23202769..23227703hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3824935
hg1924935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426318
Supporting Variants
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739671
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00228928


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