A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066502



Internal ID20633542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1242756..1252809hg38UCSC Ensembl
chr20:1223400..1233453hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3810054
hg1910054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517151
Supporting Variants
Samples
Known GenesRAD21L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066502
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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