A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419735



Internal ID198861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77608146..77611586hg38UCSC Ensembl
chrX:76863617..76867057hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg383441
hg193441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740881
Samples
Known GenesATRX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419735
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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