A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882331



Internal ID22657308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49640631..49701976hg38UCSC Ensembl
chrX:49405234..49466579hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3861346
hg1961346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452571
Samples
Known GenesPAGE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882331
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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