A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1774n209



Internal ID22827849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47019885..47023969hg38UCSC Ensembl
chr6:46987621..46991705hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg384085
hg194085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5895550, nsv5890636
Samples
Known GenesGPR110
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1774n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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