A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv37n209



Internal ID22826112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32500798..32504622hg38UCSC Ensembl
chr1:32966399..32970223hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg383825
hg193825
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5829836, nsv5829835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv37n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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