A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051253



Internal ID20618293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11928601..11933400hg38UCSC Ensembl
chr1:11988658..11993457hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317625
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0028


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