A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357886



Internal ID21015439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40084091..40084829hg38UCSC Ensembl
chr3:40125582..40126320hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38739
hg19739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211213
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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