A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424708



Internal ID203687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29175230..29227823hg38UCSC Ensembl
chrX:29193347..29245940hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3852594
hg1952594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736357
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424708
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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