A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880021



Internal ID22654991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22470973..22497425hg38UCSC Ensembl
chrX:22489090..22515542hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3826453
hg1926453
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459646
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880021
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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