A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573360



Internal ID20946431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80376773..80383523hg38UCSC Ensembl
chr7:80006089..80012839hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg386751
hg196751
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573360
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