A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558587



Internal ID331646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72685765..72685816hg38UCSC Ensembl
chr3:72734916..72734967hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg386015
hg196015
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935768
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558587
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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