A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639889



Internal ID21831936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118282505..118282505hg38UCSC Ensembl
chrX:117416468..117416468hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056069
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639889
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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