A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364334



Internal ID22590003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100079819..100083162hg38UCSC Ensembl
chr13:100732073..100735416hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg383344
hg193344
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364334
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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