A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205539



Internal ID20772579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:151280855..151620736hg38UCSC Ensembl
chr2:152137369..152477250hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38339882
hg19339882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335612
Supporting Variants
Samples
Known GenesMIR4773-1, MIR4773-2, NEB, NMI, RIF1, TNFAIP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205539
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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