A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362449



Internal ID21020002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24338372..24358467hg38UCSC Ensembl
chr4:24339995..24360090hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3820096
hg1920096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362449
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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