A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366205



Internal ID21023758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10055435..10195940hg38UCSC Ensembl
chr3:10097119..10237624hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38140506
hg19140506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208857
Samples
Known GenesBRK1, FANCD2, FANCD2OS, IRAK2, VHL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366205
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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