A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567811



Internal ID20940882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165659150..165659739hg38UCSC Ensembl
chr4:166580302..166580891hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567811
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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