A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391647



Internal ID21049200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151371864..151449207hg38UCSC Ensembl
chr4:152293016..152370359hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3877344
hg1977344
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212098
Samples
Known GenesFAM160A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391647
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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