A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531103



Internal ID20904464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18511407..18520977hg38UCSC Ensembl
chr20:18492051..18501621hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg389571
hg199571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067309
Samples
Known GenesSEC23B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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