A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648488



Internal ID21840535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132996101..132997228hg38UCSC Ensembl
chrX:132130129..132131256hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105911
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648488
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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