A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557219



Internal ID20930290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58406059..58407650hg38UCSC Ensembl
chr5:57701886..57703477hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381592
hg191592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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