A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754473



Internal ID20530333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154591327..154613096hg38UCSC Ensembl
chrX:153819590..153841349hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3821770
hg1921760
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv82n199
Supporting Variantsnssv16269425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754473
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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