A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393014



Internal ID21050567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46893801..46895600hg38UCSC Ensembl
chr4:46895818..46897617hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213708
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393014
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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