A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648076



Internal ID21840123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42943794..42949323hg38UCSC Ensembl
chrX:42803043..42808572hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg385530
hg195530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648076
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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