A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557866



Internal ID20930937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69483435..69483930hg38UCSC Ensembl
chr5:68779262..68779757hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557866
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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