A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668787



Internal ID21617092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36159810..36322017hg38UCSC Ensembl
chr19:36650712..36812919hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38162208
hg19162208
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104500
Samples
Known GenesLINC00665, LOC100134317, ZNF146, ZNF565
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668787
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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