A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196693



Internal ID20763733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130086363..130120911hg38UCSC Ensembl
chr10:131884627..131919175hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3834549
hg1934549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450947
Supporting Variants
Samples
Known GenesCTAGE7P, LINC00959
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196693
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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