A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073379



Internal ID20640419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45271152..45271727hg38UCSC Ensembl
chr21:46691067..46691642hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539032
Supporting Variants
Samples
Known GenesPOFUT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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