A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664570



Internal ID21612875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36964179..36982219hg38UCSC Ensembl
chr20:35592582..35610622hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3818041
hg1918041
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116185
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664570
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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