A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553811



Internal ID20926924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72484466..72485086hg38UCSC Ensembl
chr3:72533617..72534237hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262906
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553811
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