A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280882



Internal ID20847922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71792229..71793232hg38UCSC Ensembl
chr9:74407145..74408148hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280882
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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