A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359050



Internal ID21016603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169844662..169846378hg38UCSC Ensembl
chr3:169562450..169564166hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381717
hg191717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209201
Samples
Known GenesLRRC31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359050
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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