A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596140



Internal ID20969211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33364938..33366293hg38UCSC Ensembl
chr20:31952744..31954099hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381356
hg191356
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4444n223
Supporting Variantsnssv18251766
Samples
Known GenesCDK5RAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596140
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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