A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658283



Internal ID21606588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80355808..80355808hg38UCSC Ensembl
chr15:80648150..80648150hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097606
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658283
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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