A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607076



Internal ID20980147
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 StatusM
Merged Variantsdgv6577n223
Supporting Variantsnssv18220006
Samples
Known GenesNDUFA4, PHF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607076
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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