A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407836



Internal ID21065389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33827389..33879295hg38UCSC Ensembl
chr6:33795166..33847072hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3851907
hg1951907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407836
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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