A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389417



Internal ID21046970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113213360..113215376hg38UCSC Ensembl
chr4:114134516..114136532hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg382017
hg192017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209563
Samples
Known GenesANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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