A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360819



Internal ID21018372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185081929..185098474hg38UCSC Ensembl
chr3:184799717..184816262hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3816546
hg1916546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212177
Samples
Known GenesC3orf70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360819
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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