A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567126



Internal ID20940197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166618316..166619409hg38UCSC Ensembl
chr5:166045321..166046414hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381094
hg191094
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6020n223
Supporting Variantsnssv18268132
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567126
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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