A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110288



Internal ID22019521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23002081..23002465hg38UCSC Ensembl
chrX:23020198..23020582hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645954
Samples
Known GenesDDX53, LOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110288
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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