A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591167



Internal ID20964238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11887913..11889921hg38UCSC Ensembl
chr16:11981770..11983778hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382009
hg192009
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239857
Samples
Known GenesGSPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591167
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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