A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566489



Internal ID20939560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43323777..43326446hg38UCSC Ensembl
chr7:43363376..43366045hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382670
hg192670
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275959
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566489
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