A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373354



Internal ID22599023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62090939..62113388hg38UCSC Ensembl
chr16:62124843..62147292hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3822450
hg1922450
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373354
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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