A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363903



Internal ID21021456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51582921..51587256hg38UCSC Ensembl
chr3:51616937..51621272hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg384336
hg194336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209974
Samples
Known GenesRAD54L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363903
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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