A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530590



Internal ID20903951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4166365..4168935hg38UCSC Ensembl
chr20:4147012..4149582hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382571
hg192571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202269
Samples
Known GenesSMOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530590
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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