A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220006



Internal ID20787046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10873758..10995065hg38UCSC Ensembl
chr7:10913385..11034692hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38121308
hg19121308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607076
Supporting Variants
Samples
Known GenesNDUFA4, PHF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220006
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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