A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370320



Internal ID21027873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68567314..69424179hg38UCSC Ensembl
chr3:68616465..69473330hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38856866
hg19856866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213012
Samples
Known GenesARL6IP5, EOGT, FAM19A4, FRMD4B, LMOD3, MIR3136, TMF1, UBA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370320
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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