A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609145



Internal ID20982216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127756799..127799389hg38UCSC Ensembl
chr6:128077944..128120534hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3842591
hg1942591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215527
Samples
Known GenesTHEMIS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609145
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