A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259114



Internal ID20468302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135116140..135256382hg38UCSC Ensembl
chrX:134250066..134390330hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38140243
hg19140265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767049
Supporting Variants
Samples
Known GenesCXorf48, LINC00633, LOC100287728
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259114
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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