A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421828



Internal ID200890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105276653..105322856hg38UCSC Ensembl
chrX:104521337..104567541hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3846204
hg1946205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737182
Samples
Known GenesIL1RAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421828
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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