A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647686



Internal ID21839733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9404159..9414708hg38UCSC Ensembl
chrX:9372199..9382748hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3810550
hg1910550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647686
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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