A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419433



Internal ID198563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101851755..101854167hg38UCSC Ensembl
chrX:101106727..101109139hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg382413
hg192413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741744
Samples
Known GenesNXF5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419433
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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