A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225828



Internal ID20792868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96210201..96220878hg38UCSC Ensembl
chr6:96658077..96668754hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3810678
hg1910678
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404225
Supporting Variants
Samples
Known GenesFUT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225828
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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