A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201059



Internal ID20768099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175095101..175111600hg38UCSC Ensembl
chr1:175064237..175080736hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3816500
hg1916500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317697
Supporting Variants
Samples
Known GenesTNN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00724


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