A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346498



Internal ID21004051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145660493..145661081hg38UCSC Ensembl
chr2:146418061..146418649hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346498
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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