A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503889



Internal ID20877147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49362501..49369400hg38UCSC Ensembl
chr15:49654698..49661597hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182828
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503889
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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