A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv15n209



Internal ID22826090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6398533..6399767hg38UCSC Ensembl
chr1:6458593..6459827hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5830610, nsv5830423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv15n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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