A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801274



Internal ID21246612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21166096..21166096hg38UCSC Ensembl
chr1:21492589..21492589hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681622
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801274
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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