A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219581



Internal ID20786621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42332200..42333029hg38UCSC Ensembl
chr13:42906336..42907165hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219581
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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