A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346789



Internal ID21004342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208044116..208045811hg38UCSC Ensembl
chr2:208908840..208910535hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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