A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567486



Internal ID20940557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2485490..2486081hg38UCSC Ensembl
chr7:2525124..2525715hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272752
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567486
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