A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421347



Internal ID200424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19928471..19930103hg38UCSC Ensembl
chrX:19946589..19948221hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg381633
hg191633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739549
Samples
Known GenesCXorf23
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421347
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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