A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221939



Internal ID20788979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66598467..66603213hg38UCSC Ensembl
chr7:66063454..66068200hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg384747
hg194747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221939
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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