A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880507



Internal ID22655477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153542049..153542119hg38UCSC Ensembl
chrX:152807507..152807577hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435563
Samples
Known GenesATP2B3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880507
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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