A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596532



Internal ID20969603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2216357..2216940hg38UCSC Ensembl
chr20:2197003..2197586hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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