A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518930



Internal ID20892291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18288101..18289100hg38UCSC Ensembl
chr20:18268745..18269744hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066683
Samples
Known GenesZNF133
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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