A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218526



Internal ID20785566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62164112..62165031hg38UCSC Ensembl
chr13:62738245..62739164hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584285
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218526
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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