A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv659n223



Internal ID22803627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26563901..26601104hg38UCSC Ensembl
chr10:26852830..26890033hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3837204
hg1937204
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6454414, nsv6453912
Samples
Known GenesAPBB1IP, LINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv659n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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