A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv42n209



Internal ID22826117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46584338..46587560hg38UCSC Ensembl
chr1:47050010..47053232hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg383223
hg193223
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5830218, nsv5830219
Samples
Known GenesMKNK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv42n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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