A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742397



Internal ID166063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133221220..133222166hg38UCSC Ensembl
chrX:132355248..132356194hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38947
hg19947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742397
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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