A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857034



Internal ID22631969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18334549..18339042hg38UCSC Ensembl
chrUn_gl000212:163301..167794hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384494
hg194494
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457986, nssv17464647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857034
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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