A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362855



Internal ID21020408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111857801..111863500hg38UCSC Ensembl
chr3:111576648..111582347hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207847
Samples
Known GenesPHLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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