A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343061



Internal ID21000614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183610901..183776800hg38UCSC Ensembl
chr2:184475629..184641527hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38165900
hg19165899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343061
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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