A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2816236



Internal ID21261574
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 StatusM
Merged Variants
Supporting Variantsnssv13707416
Samples
Known GenesEBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2816236
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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