A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356586



Internal ID21014139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68976231..69042996hg38UCSC Ensembl
chr3:69025382..69092147hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3866766
hg1966766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211218
Samples
Known GenesEOGT, TMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356586
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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