A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362636



Internal ID21020189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188880124..188882886hg38UCSC Ensembl
chr3:188597912..188600674hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382763
hg192763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212237
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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