A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351659



Internal ID21009212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47880987..48143437hg38UCSC Ensembl
chr2:48108126..48370576hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38262451
hg19262451
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209834
Samples
Known GenesFBXO11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351659
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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