A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387990



Internal ID22445860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77334769..77334834hg38UCSC Ensembl
chr16:77368666..77368731hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968441
Supporting Variants
Samples
Known GenesADAMTS18
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387990
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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