A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373992



Internal ID21031545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120545493..120546080hg38UCSC Ensembl
chr3:120264340..120264927hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373992
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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