A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538313



Internal ID20911630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33391701..33410800hg38UCSC Ensembl
chr21:34764007..34783106hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3819100
hg1919100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206664
Samples
Known GenesIFNGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538313
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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