A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204300



Internal ID20771340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6542838..6559139hg38UCSC Ensembl
chr1:6602898..6619199hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3816302
hg1916302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324113
Supporting Variants
Samples
Known GenesNOL9, TAS1R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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