A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369692



Internal ID21027245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35467901..35499100hg38UCSC Ensembl
chr4:35469523..35500722hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3831200
hg1931200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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