A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390477



Internal ID21048030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87859601..87867500hg38UCSC Ensembl
chr4:88780753..88788652hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390477
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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