A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3791n54



Internal ID22771686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79638233..79648520hg38UCSC Ensembl
chr14:80104576..80114863hg19UCSC Ensembl
chr14:79174329..79184616hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3810288
hg1910288
hg1810288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565249, nsv565250
Samples
Known GenesNRXN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3791n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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