A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641462



Internal ID21833509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94868797..94868797hg38UCSC Ensembl
chrX:94123796..94123796hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg385931
hg195931
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056928
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641462
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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