A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408169



Internal ID21065722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95440173..95440696hg38UCSC Ensembl
chr5:94775877..94776400hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215029
Samples
Known GenesFAM81B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408169
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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