A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593519



Internal ID20966590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11269617..11287264hg38UCSC Ensembl
chr16:11363474..11381121hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817648
hg1917648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239827
Samples
Known GenesPRM1, PRM2, PRM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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