A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558846



Internal ID20931917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146183222..146184323hg38UCSC Ensembl
chr5:145562785..145563886hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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