A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707416



Internal ID21229207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26005351..26005351hg38UCSC Ensembl
chr8:25862867..25862867hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2816236
Supporting Variants
Samples
Known GenesEBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707416
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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