A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422021



Internal ID201077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5821597..5827606hg38UCSC Ensembl
chrX:5739638..5745647hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg386010
hg196010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422021
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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