A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424165



Internal ID203164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101423041..101425586hg38UCSC Ensembl
chrX:100678029..100680574hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg382546
hg192546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741725
Samples
Known GenesARMCX4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424165
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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