A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597520



Internal ID20970591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59058234..59058701hg38UCSC Ensembl
chr20:57633289..57633756hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597520
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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