A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554817



Internal ID20927907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:83315367..83317127hg38UCSC Ensembl
chr3:83364518..83366278hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg381761
hg191761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554817
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer