A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362710



Internal ID21020263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149467904..149477130hg38UCSC Ensembl
chr3:149185691..149194917hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg389227
hg199227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211404
Samples
Known GenesTM4SF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362710
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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