A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422876



Internal ID201906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133524157..133529259hg38UCSC Ensembl
chrX:132658185..132663287hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg385103
hg195103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422876
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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