A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642343



Internal ID21834390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153289402..153289402hg38UCSC Ensembl
chrX:152554860..152554860hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053860
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642343
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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