A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862980



Internal ID22637915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40005422..40007066hg38UCSC Ensembl
chr13:40579559..40581203hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381645
hg191645
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862980
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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