A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1345n209



Internal ID22827420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14375536..14378035hg38UCSC Ensembl
chr21:15747857..15750356hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5887307, nsv5884406
Samples
Known GenesHSPA13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1345n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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