A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424975



Internal ID203949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101121503..101121565hg38UCSC Ensembl
chrX:100376492..100376554hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741709
Samples
Known GenesCENPI
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424975
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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