A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362821



Internal ID21020374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153269119..153276684hg38UCSC Ensembl
chr3:152986908..152994473hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg387566
hg197566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362821
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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