A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351989



Internal ID21009542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28389901..28391400hg38UCSC Ensembl
chr2:28612768..28614267hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209151
Samples
Known GenesFLJ31356
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351989
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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