A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657094



Internal ID21605399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143052..62143052hg38UCSC Ensembl
chr11:61910524..61910524hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074888
SamplesHG00731
Known GenesINCENP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657094
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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