A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532126



Internal ID20905487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6001801..6009400hg38UCSC Ensembl
chr20:5982447..5990046hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203356
Samples
Known GenesCRLS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532126
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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