A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793778



Internal ID21239116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31723080..31723080hg38UCSC Ensembl
chr13:32297217..32297217hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793778
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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