A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655330



Internal ID21603635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73897370..73897370hg38UCSC Ensembl
chr11:73608415..73608415hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076046
SamplesHG03371
Known GenesPAAF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655330
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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