A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346809



Internal ID21004362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109027233..109034315hg38UCSC Ensembl
chr2:109643689..109650771hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg387083
hg197083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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