A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353881



Internal ID21011434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203205001..203209900hg38UCSC Ensembl
chr2:204069724..204074623hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208072
Samples
Known GenesNBEAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353881
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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