A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655095



Internal ID21603400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134138440..134138440hg38UCSC Ensembl
chr11:134008335..134008335hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381387
hg191387
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073154, nssv17073153
SamplesHG03486, NA19238
Known GenesJAM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655095
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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