A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560505



Internal ID333512
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 StatusM
Merged Variants
Supporting Variantsnssv17742462
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)nsv5560505
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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