A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374147



Internal ID21031700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1398501..1403800hg38UCSC Ensembl
chr4:1392289..1397588hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374147
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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