A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404882



Internal ID21062435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86084367..86104353hg38UCSC Ensembl
chr6:86794085..86814071hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3819987
hg1919987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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