A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861791



Internal ID22636726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18236536..18254500hg38UCSC Ensembl
chrUn_gl000212:65288..83252hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3817965
hg1917965
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457893, nssv17453503, nssv17465924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861791
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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