A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486901



Internal ID21144454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107782101..107783900hg38UCSC Ensembl
chr13:108434449..108436248hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196454
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486901
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