A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229390



Internal ID20796430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98253199..98253664hg38UCSC Ensembl
chr7:97882511..97882976hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229390
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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