A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569493



Internal ID20942564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112476963..112477419hg38UCSC Ensembl
chr5:111812660..111813116hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569493
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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