A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351455



Internal ID21009008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113466701..113513700hg38UCSC Ensembl
chr2:114224278..114271277hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3847000
hg1947000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4082n223
Supporting Variantsnssv18206497
Samples
Known GenesCBWD2, FOXD4L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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