A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766471



Internal ID20542331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154555895..154648545hg38UCSC Ensembl
chrX:153784110..153876819hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3892651
hg1992710
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262863
Samples
Known GenesCTAG1A, CTAG1B, FAM223A, FAM223B, IKBKG
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766471
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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