A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422638



Internal ID201679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101313872..101327958hg38UCSC Ensembl
chrX:100568860..100582946hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3814087
hg1914087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422638
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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