A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548713



Internal ID20921896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33285385..33323718hg38UCSC Ensembl
chr21:34657690..34696023hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3838334
hg1938334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206661
Samples
Known GenesIL10RB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548713
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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