A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv53n209



Internal ID22826128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110455865..110458986hg38UCSC Ensembl
chr1:110998487..111001608hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg383122
hg193122
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5827707, nsv5827797
Samples
Known GenesPROK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv53n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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