A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388614



Internal ID21046167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:162159101..162249900hg38UCSC Ensembl
chr4:163080253..163171052hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3890800
hg1990800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5542n223
Supporting Variantsnssv18211152
Samples
Known GenesFSTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388614
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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