A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551113



Internal ID20924253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41043267..41053364hg38UCSC Ensembl
chr20:39671907..39682004hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3810098
hg1910098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067603
Samples
Known GenesTOP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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