A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv913n223



Internal ID22803881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131042201..131592500hg38UCSC Ensembl
chr10:132840464..133381404hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38550300
hg19540941
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6450442, nsv6438086
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv913n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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