A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv761n209



Internal ID22826836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81633734..81651196hg38UCSC Ensembl
chr15:81926075..81943537hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3817463
hg1917463
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5847567, nsv5852746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv761n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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