A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066206



Internal ID20633246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99888092..99888520hg38UCSC Ensembl
chr1:100353648..100354076hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331279
Supporting Variants
Samples
Known GenesAGL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00111


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