A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597756



Internal ID20970827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31659675..31660838hg38UCSC Ensembl
chr20:30247478..30248641hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597756
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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