A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641136



Internal ID21833183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154591073..154607498hg38UCSC Ensembl
chrX:153819336..153835751hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3816426
hg1916416
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641136
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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