A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv889n223



Internal ID22803857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113439452..113787342hg38UCSC Ensembl
chr10:115199211..115547101hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38347891
hg19347891
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6454807, nsv6443022
Samples
Known GenesCASP7, HABP2, MIR4483, NRAP, PLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv889n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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