A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222639



Internal ID20789679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138429356..138438081hg38UCSC Ensembl
chr7:138114101..138122826hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg388726
hg198726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422339
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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