A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595206



Internal ID20968277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56707218..56708338hg38UCSC Ensembl
chr16:56741130..56742250hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595206
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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