A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758040



Internal ID20533900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55478889..55494317hg38UCSC Ensembl
chrX:55505322..55520750hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3815429
hg1915429
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260795
Samples
Known GenesUSP51
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758040
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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