A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386893



Internal ID22444763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80436147..80437612hg38UCSC Ensembl
chr13:81010282..81011747hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381466
hg191466
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979037
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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