A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767049



Internal ID20542909
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 StatusM
Merged Variants
Supporting Variantsnssv16259114
Samples
Known GenesCXorf48, LINC00633, LOC100287728
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767049
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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