A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858762



Internal ID22633697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18205257..18208517hg38UCSC Ensembl
chrUn_gl000212:34009..37269hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383261
hg193261
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469268, nssv17452244, nssv17454740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858762
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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