A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373183



Internal ID21030736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39983653..40014506hg38UCSC Ensembl
chr3:40025144..40055997hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3830854
hg1930854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211212
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373183
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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