A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2791779



Internal ID21237117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108215428..108215428hg38UCSC Ensembl
chr13:108867776..108867776hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683262
Samples
Known GenesLIG4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2791779
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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