A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515854



Internal ID22573816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155996730..156006609hg38UCSC Ensembl
chrX:155226395..155236274hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg389880
hg199880
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970181
Supporting Variants
Samples
Known GenesIL9R
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515854
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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