A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857081



Internal ID22632016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18234836..18236735hg38UCSC Ensembl
chrUn_gl000212:63588..65487hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461646, nssv17452936, nssv17462170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857081
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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