A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852060



Internal ID22626995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18208723..18211061hg38UCSC Ensembl
chrUn_gl000212:37475..39813hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382339
hg192339
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452228, nssv17455417, nssv17457810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852060
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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