A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646546



Internal ID21838593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151917389..151917498hg38UCSC Ensembl
chrX:151085861..151085970hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106673
Supporting Variants
Samples
Known GenesMAGEA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646546
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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