A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737167



Internal ID160833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104875821..104877615hg38UCSC Ensembl
chrX:104120502..104122296hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg381795
hg191795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424115
Supporting Variants
Samples
Known GenesIL1RAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737167
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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