A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609027



Internal ID20982098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66543746..66551011hg38UCSC Ensembl
chr7:66008733..66015998hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg387266
hg197266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609027
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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