A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345113



Internal ID21002666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203629978..203638325hg38UCSC Ensembl
chr2:204494701..204503048hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg388348
hg198348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345113
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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