A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370863



Internal ID22596532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66102860..66331284hg38UCSC Ensembl
chr16:66136763..66365187hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38228425
hg19228425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370863
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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