A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692409



Internal ID21214263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43423115..43423115hg38UCSC Ensembl
chr10:43918563..43918563hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381936
hg191936
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788940
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692409
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.769231


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