A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621524



Internal ID21569829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206097964..206097964hg38UCSC Ensembl
chr2:206962688..206962688hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109982
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621524
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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