A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066208



Internal ID20633248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99921901..99922700hg38UCSC Ensembl
chr1:100387457..100388256hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332864
Supporting Variants
Samples
Known GenesAGL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066208
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00119


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