A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419096



Internal ID198244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5563758..5578517hg38UCSC Ensembl
chrX:5481799..5496558hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3814760
hg1914760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419096
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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