A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607097



Internal ID21555402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184628170..184628170hg38UCSC Ensembl
chr3:184345958..184345958hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132743
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607097
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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