A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6513n223



Internal ID22809481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167927901..168236400hg38UCSC Ensembl
chr6:168328581..168637080hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38308500
hg19308500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6600778, nsv6612973, nsv6618890, nsv6610781
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6513n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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