A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968027



Internal ID22742962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36588444..37065469hg38UCSC Ensembl
chrX:36606518..37083542hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38477026
hg19477025
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464191
Samples
Known GenesFAM47C, FTH1P18
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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