A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654457



Internal ID21602762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77196295..77196295hg38UCSC Ensembl
chr16:77230192..77230192hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086556
SamplesHG00731
Known GenesMON1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654457
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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