A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320516



Internal ID20853615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149557601..149559100hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320516
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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