A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593931



Internal ID20967002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75721760..75738322hg38UCSC Ensembl
chr16:75755658..75772220hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3816563
hg1916563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593931
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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