A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225517



Internal ID20792557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98547995..98548576hg38UCSC Ensembl
chr7:98177307..98177888hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225517
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.61483


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