A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371515



Internal ID22597184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:36334708..36347927hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3813220
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371515
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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