A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199300



Internal ID20766340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11373754..11374511hg38UCSC Ensembl
chr1:11433811..11434568hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.02039


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