A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374589



Internal ID21032142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67658647..67659715hg38UCSC Ensembl
chr3:67709071..67710139hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374589
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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