A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349869



Internal ID21007422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199599601..199605400hg38UCSC Ensembl
chr2:200464324..200470123hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349869
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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