A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546109



Internal ID20919328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31664226..31664869hg38UCSC Ensembl
chr21:33036539..33037182hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206066
Samples
Known GenesSOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546109
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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