A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596332



Internal ID20969403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33926865..33928716hg38UCSC Ensembl
chr20:32514671..32516522hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381852
hg191852
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4448n223
Supporting Variantsnssv18251798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596332
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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