A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382064



Internal ID21039617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120917301..120925600hg38UCSC Ensembl
chr4:121838456..121846755hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210212
Samples
Known GenesPRDM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382064
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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