A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655423



Internal ID21603728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127942193..127942193hg38UCSC Ensembl
chr11:127812088..127812088hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073473
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655423
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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