A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568789



Internal ID20941860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10280833..10282528hg38UCSC Ensembl
chr5:10280945..10282640hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5637n223
Supporting Variantsnssv18266463
Samples
Known GenesCMBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568789
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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