A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337450



Internal ID20995003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174738747..174769722hg38UCSC Ensembl
chr2:175603475..175634450hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3830976
hg1930976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207431
Samples
Known GenesCHRNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337450
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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