A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455235



Internal ID22513112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24284726..24286052hg38UCSC Ensembl
chrX:24302843..24304169hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg381327
hg191327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455235
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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