A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280232



Internal ID20847272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16675432..16675931hg38UCSC Ensembl
chr9:16675430..16675929hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565059
Supporting Variants
Samples
Known GenesBNC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280232
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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