A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801269



Internal ID21246607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20807953..20807953hg38UCSC Ensembl
chr1:21134446..21134446hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682671
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801269
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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