A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858042



Internal ID22632977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67780700..67791572hg38UCSC Ensembl
chr13:68354832..68365704hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3810873
hg1910873
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858042
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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