A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450735



Internal ID21108288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5597422..5628213hg38UCSC Ensembl
chr10:5639385..5670176hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3830792
hg1930792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450735
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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