A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379137



Internal ID21036690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169561409..169638987hg38UCSC Ensembl
chr4:170482560..170560138hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3877579
hg1977579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213868
Samples
Known GenesCLCN3, NEK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379137
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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