A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347865



Internal ID21005418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25351600..25357783hg38UCSC Ensembl
chr2:25574469..25580652hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg386184
hg196184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347865
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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