A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639094



Internal ID21831141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103772857..103772857hg38UCSC Ensembl
chrX:103027785..103027785hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg383350
hg193350
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639094
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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