A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861796



Internal ID22636731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18206399..18208517hg38UCSC Ensembl
chrUn_gl000212:35151..37269hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464715, nssv17463073, nssv17457424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861796
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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