A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800979



Internal ID21246318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20981569..20981630hg38UCSC Ensembl
chr1:21308062..21308123hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693913
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800979
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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