A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433624



Internal ID212331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101431567..101433435hg38UCSC Ensembl
chrX:100686555..100688423hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg381869
hg191869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741726
Samples
Known GenesARMCX4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433624
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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