A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382306



Internal ID21039859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110200873..110212536hg38UCSC Ensembl
chr4:111122029..111133692hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3811664
hg1911664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382306
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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