A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373868



Internal ID21031421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123452069..123461244hg38UCSC Ensembl
chr3:123170916..123180091hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg389176
hg199176
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373868
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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