A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059217



Internal ID20626257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2285870..2294908hg38UCSC Ensembl
chr1:2217309..2226347hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg389039
hg199039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317747
Supporting Variants
Samples
Known GenesSKI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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