A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388910



Internal ID21046463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16533122..16538788hg38UCSC Ensembl
chr5:16533231..16538897hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg385667
hg195667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215979
Samples
Known GenesFAM134B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388910
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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