A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221966



Internal ID20789006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47253801..47255900hg38UCSC Ensembl
chr7:47293399..47295498hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221966
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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