A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342299



Internal ID20999852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:54693901..54726900hg38UCSC Ensembl
chr2:54921038..54954037hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3833000
hg1933000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209923
Samples
Known GenesEML6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342299
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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