A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069007



Internal ID20636047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49605850..49618155hg38UCSC Ensembl
chr20:48222387..48234692hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3812306
hg1912306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542937
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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