A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643928



Internal ID21835975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129849679..129849785hg38UCSC Ensembl
chrX:128983655..128983761hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643928
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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