A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372607



Internal ID21030160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41194601..41202400hg38UCSC Ensembl
chr3:41236092..41243891hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208642
Samples
Known GenesCTNNB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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