A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959886



Internal ID22734905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133057866..133057866hg38UCSC Ensembl
chrX:132191894..132191894hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439726
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959886
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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