A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597784



Internal ID20970855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37248154..37249293hg38UCSC Ensembl
chr20:35876557..35877696hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4456n223
Supporting Variantsnssv18254353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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