A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864231



Internal ID22639166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114349760..114351883hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382124
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467013, nssv17463638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864231
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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