A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367952



Internal ID21025505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109424902..109455806hg38UCSC Ensembl
chr3:109143749..109174653hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3830905
hg1930905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207225
Samples
Known GenesFLJ25363
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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