A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660196



Internal ID21608501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95322055..95322055hg38UCSC Ensembl
chr11:95055219..95055219hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076866
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660196
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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