A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350372



Internal ID21007925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164665963..164668142hg38UCSC Ensembl
chr2:165522473..165524652hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382180
hg192180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350372
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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