A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437132



Internal ID22495002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101431564..101433434hg38UCSC Ensembl
chrX:100686552..100688422hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg381871
hg191871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867889
Supporting Variants
Samples
Known GenesARMCX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437132
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