A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542886



Internal ID20916137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31219027..31265233hg38UCSC Ensembl
chr21:32591343..32637549hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3846207
hg1946207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206057
Samples
Known GenesTIAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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