A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361479



Internal ID21019032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94927526..94978080hg38UCSC Ensembl
chr3:94646370..94696924hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3850555
hg1950555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210809
Samples
Known GenesLINC00879
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361479
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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