A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv686n223



Internal ID22803654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34881089..35053653hg38UCSC Ensembl
chr10:35170017..35342581hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38172565
hg19172565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6435707, nsv6450169
Samples
Known GenesCUL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv686n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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