A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066147



Internal ID20633187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99238170..99244385hg38UCSC Ensembl
chr1:99703726..99709941hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg386216
hg196216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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