A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575478



Internal ID20948549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97878029..97878472hg38UCSC Ensembl
chr9:100640311..100640754hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575478
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