A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369427



Internal ID21026980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84781811..84818350hg38UCSC Ensembl
chr3:84830962..84867501hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3836540
hg1936540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210121
Samples
Known GenesLINC00971
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369427
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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