A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228964



Internal ID20796004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2323941..2343495hg38UCSC Ensembl
chr7:2363576..2383130hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3819555
hg1919555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228964
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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