A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366032



Internal ID21023585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48129355..48148690hg38UCSC Ensembl
chr3:48170845..48190180hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3819336
hg1919336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4865n223
Supporting Variantsnssv18209326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366032
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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