A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1213n223



Internal ID22804181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65311837..65328663hg38UCSC Ensembl
chr11:65079308..65096134hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3816827
hg1916827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6467454, nsv6466368
Samples
Known GenesCDC42EP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1213n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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