A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646070



Internal ID21838117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104148100..104148483hg38UCSC Ensembl
chrX:103392781..103393164hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102299
Supporting Variants
Samples
Known GenesSLC25A53
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646070
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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