A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259418



Internal ID20468636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74435472..74435472hg38UCSC Ensembl
chrX:73655307..73655307hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740860
Supporting Variants
Samples
Known GenesSLC16A2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259418
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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