A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433225



Internal ID211948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15964244..16616050hg38UCSC Ensembl
chrX:15982367..16634173hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38651807
hg19651807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739412
Samples
Known GenesCTPS2, GRPR, MAGEB17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433225
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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