A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218896



Internal ID20785936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115978064..115998333hg38UCSC Ensembl
chr7:115618118..115638387hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3820270
hg1920270
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617202
Supporting Variants
Samples
Known GenesTFEC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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