A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280588



Internal ID20847629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35231982..35232178hg38UCSC Ensembl
chr9:35231979..35232175hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566248
Supporting Variants
Samples
Known GenesUNC13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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