A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664944



Internal ID21613251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:343633..343984hg38UCSC Ensembl
chrX:304368..304719hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167262
SamplesHG03486
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664944
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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