A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458472



Internal ID22516355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:769153..786138hg38UCSC Ensembl
chrX:729888..746873hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3816986
hg1916986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979904
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458472
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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