A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv148n209



Internal ID22826223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14608243..14611587hg38UCSC Ensembl
chr10:14650242..14653586hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383345
hg193345
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5856274, nsv5857115
Samples
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv148n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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