A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621161



Internal ID21569466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72405815..72405815hg38UCSC Ensembl
chr3:72454966..72454966hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139051
SamplesHG03125
Known GenesRYBP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621161
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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