A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624504



Internal ID21572809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105663102..105663102hg38UCSC Ensembl
chr3:105381946..105381946hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121066
SamplesNA19238
Known GenesCBLB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624504
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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