A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424698



Internal ID203677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24951242..24951307hg38UCSC Ensembl
chrX:24969359..24969424hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739757
Samples
Known GenesPOLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424698
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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