A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521737



Internal ID20895098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:596427..614460hg38UCSC Ensembl
chr20:577071..595104hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3818034
hg1918034
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203350
Samples
Known GenesTCF15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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