A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646021



Internal ID21838068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3093130..3102714hg38UCSC Ensembl
chrX:3011171..3020755hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg389585
hg199585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107583
Supporting Variants
Samples
Known GenesARSF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646021
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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