A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648642



Internal ID21840689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107742262..107742315hg38UCSC Ensembl
chrX:106985492..106985545hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106092
Supporting Variants
Samples
Known GenesTSC22D3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648642
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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