A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608218



Internal ID20981289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83439683..83461142hg38UCSC Ensembl
chr7:83068999..83090458hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3821460
hg1921460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227791
Samples
Known GenesSEMA3E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608218
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