A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374335



Internal ID21031888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15108796..15118346hg38UCSC Ensembl
chr3:15150303..15159853hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg389551
hg199551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374335
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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