A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655371



Internal ID21603676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69936060..69936060hg38UCSC Ensembl
chr11:69782166..69782166hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075815
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655371
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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