A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102299



Internal ID22011535
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 StatusM
Merged Variants
Supporting Variantsnssv17646070
Samples
Known GenesSLC25A53
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102299
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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