A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644697



Internal ID21593002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67118461..67118461hg38UCSC Ensembl
chr11:66885932..66885932hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075307
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644697
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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