A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379941



Internal ID22437811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79657511..79660753hg38UCSC Ensembl
chr16:79691408..79694650hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379941
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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