A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355079



Internal ID21012632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26811477..26847274hg38UCSC Ensembl
chr2:27034345..27070142hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3835798
hg1935798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209134
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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