A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590087



Internal ID20963158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13054260..13056164hg38UCSC Ensembl
chr16:13148117..13150021hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381905
hg191905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239899
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590087
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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