A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566351



Internal ID20939422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147865845..147872191hg38UCSC Ensembl
chr5:147245408..147251754hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386347
hg196347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566351
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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