A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390474



Internal ID21048027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170022701..170029200hg38UCSC Ensembl
chr4:170943852..170950351hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213874
Samples
Known GenesMFAP3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390474
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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