A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738082



Internal ID161748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153598370..153602156hg38UCSC Ensembl
chrX:152863828..152867611hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg383787
hg193784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424612
Supporting Variants
Samples
Known GenesFAM58A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738082
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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