A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615295



Internal ID21563600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100520062..100520062hg38UCSC Ensembl
chr2:101136524..101136524hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107428
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615295
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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