A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392703



Internal ID21050256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98891601..98896000hg38UCSC Ensembl
chr4:99812752..99817151hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214405
Samples
Known GenesEIF4E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392703
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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