A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597923



Internal ID20970994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43496543..43497678hg38UCSC Ensembl
chr20:42125183..42126318hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381136
hg191136
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252067
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597923
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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