A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556836



Internal ID20929907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32885443..32886557hg38UCSC Ensembl
chr5:32885549..32886663hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381115
hg191115
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556836
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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