A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591467



Internal ID20964538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19360647..19361382hg38UCSC Ensembl
chr16:19371969..19372704hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591467
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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