A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422339



Internal ID21079892
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 StatusM
Merged Variants
Supporting Variantsnssv18222639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422339
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer