A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2792158



Internal ID21237496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109489289..109489289hg38UCSC Ensembl
chr13:110141636..110141636hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13694189, nssv13685489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2792158
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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