A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648455



Internal ID21840502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138865420..138865498hg38UCSC Ensembl
chrX:137947582..137947660hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101154
Supporting Variants
Samples
Known GenesFGF13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648455
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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