A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767161



Internal ID20543021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146808256..146816233hg38UCSC Ensembl
chrX:145889774..145897751hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg387978
hg197978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294704
Samples
Known GenesCXorf51A, CXorf51B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767161
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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