A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354973



Internal ID21012526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220813501..220815800hg38UCSC Ensembl
chr2:221678221..221680520hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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