A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449472



Internal ID21107025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92820829..92823553hg38UCSC Ensembl
chr10:94580586..94583310hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg382725
hg192725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449472
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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