A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280897



Internal ID20847937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72017819..72018317hg38UCSC Ensembl
chr9:74632735..74633233hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280897
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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