A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052861



Internal ID20619901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166055896..166056245hg38UCSC Ensembl
chr1:166025133..166025482hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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