A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642661



Internal ID21834708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:108040606..108042004hg38UCSC Ensembl
chrX:107283836..107285234hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg381399
hg191399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642661
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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