A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979904



Internal ID22754839
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 StatusM
Merged Variants
Supporting Variantsnssv17458472
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979904
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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