A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354645



Internal ID21012198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166845084..166847399hg38UCSC Ensembl
chr2:167701594..167703909hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382316
hg192316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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