A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059970



Internal ID20627010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28647644..28650322hg38UCSC Ensembl
chr1:28974156..28976834hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382679
hg192679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318371
Supporting Variants
Samples
Known GenesRNU11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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