A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389268



Internal ID22447138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34285151..37946447hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383661297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389268
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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