A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276101



Internal ID20485319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:98524364..98524364hg38UCSC Ensembl
chrX:97779362..97779362hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733970
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276101
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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