A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232101



Internal ID20799141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36816482..36817566hg38UCSC Ensembl
chr13:37390619..37391703hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381085
hg191085
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232101
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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