A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742462



Internal ID166128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135097530..135423178hg38UCSC Ensembl
chrX:134231560..134557103hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38325649
hg19325544
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560505
Supporting Variants
Samples
Known GenesCXorf48, LINC00086, LINC00087, LINC00633, LOC100287728, LOC100506790, ZNF449, ZNF75D
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742462
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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