A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374213



Internal ID21031766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51529044..51578664hg38UCSC Ensembl
chr3:51563060..51612680hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3849621
hg1949621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209973
Samples
Known GenesRAD54L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374213
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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