A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426022



Internal ID204968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42912418..42931150hg38UCSC Ensembl
chrX:42771667..42790399hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3818733
hg1918733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426022
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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