A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742401



Internal ID166067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133392561..133392964hg38UCSC Ensembl
chrX:132526589..132526992hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556517
Supporting Variants
Samples
Known GenesGPC4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742401
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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