A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433202



Internal ID211927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20216430..20216809hg38UCSC Ensembl
chrX:20234548..20234927hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739556
Samples
Known GenesRPS6KA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433202
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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