A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375046



Internal ID21032599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149318058..149319228hg38UCSC Ensembl
chr3:149035845..149037015hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381171
hg191171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211400
Samples
Known GenesTM4SF18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375046
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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