A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230255



Internal ID20797295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98519492..98534733hg38UCSC Ensembl
chr7:98148804..98164045hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3815242
hg1915242
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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