A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294106



Internal ID20503324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149600641..149768713hg38UCSC Ensembl
chrX:148682305..148850374hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38168073
hg19168070
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754201
Supporting Variants
Samples
Known GenesMAGEA11, TMEM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294106
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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