A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073262



Internal ID20640302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43947247..43948434hg38UCSC Ensembl
chr21:45367128..45368315hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381188
hg191188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546656
Supporting Variants
Samples
Known GenesAGPAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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