A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230333



Internal ID20797373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106485596..106492030hg38UCSC Ensembl
chr7:106126042..106132476hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg386435
hg196435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230333
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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