A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661777



Internal ID21610082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66349791..66349791hg38UCSC Ensembl
chr11:66117262..66117262hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075440
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661777
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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