A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363447



Internal ID21021000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105832301..105928698hg38UCSC Ensembl
chr3:105551145..105647545hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3896398
hg1996401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208930
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363447
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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