A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280915



Internal ID20847955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72327739..72327840hg38UCSC Ensembl
chr9:74942655..74942756hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280915
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer