A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221007



Internal ID20788047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86247507..86327507hg38UCSC Ensembl
chr6:86957225..87037225hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3880001
hg1980001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398923
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221007
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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