A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569162



Internal ID20942233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72446809..72448390hg38UCSC Ensembl
chr9:75061725..75063306hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7828n223
Supporting Variantsnssv18280923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569162
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