A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357966



Internal ID21015519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38839327..38851828hg38UCSC Ensembl
chr3:38880818..38893319hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3812502
hg1912502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211202
Samples
Known GenesSCN11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357966
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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