A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645954



Internal ID21838001
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 StatusS
Merged Variantsnsv6110288
Supporting Variants
Samples
Known GenesDDX53, LOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645954
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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