A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339533



Internal ID20997086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42943299..43112105hg38UCSC Ensembl
chr2:43170439..43339244hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38168807
hg19168806
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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