A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407286



Internal ID21064839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96519151..96538869hg38UCSC Ensembl
chr5:95854855..95874573hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3819719
hg1919719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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