A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372983



Internal ID21030536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107110954..107117243hg38UCSC Ensembl
chr3:106829801..106836090hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg386290
hg196290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207198
Samples
Known GenesLINC00882
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372983
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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