A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254362



Internal ID20821402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37683235..37683606hg38UCSC Ensembl
chr20:36311637..36312008hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596584
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254362
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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