A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539140



Internal ID20912447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33451025..33466962hg38UCSC Ensembl
chr21:34823332..34839269hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3815938
hg1915938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206665
Samples
Known GenesTMEM50B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539140
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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