A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335612



Internal ID20993165
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 StatusM
Merged Variantsdgv4154n223
Supporting Variantsnssv18205539
Samples
Known GenesMIR4773-1, MIR4773-2, NEB, NMI, RIF1, TNFAIP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335612
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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