A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979545



Internal ID22754480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89156412..89373872hg38UCSC Ensembl
chr16:89222820..89440280hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38217461
hg19217461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373226
Samples
Known GenesANKRD11, CDH15, LINC00304, LOC100287036, LOC400558, SLC22A31, ZNF778
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979545
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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