A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155036



Internal ID22085541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:78694842..78699265hg38UCSC Ensembl
Outerchr14:78690697..78699982hg38UCSC Ensembl
Innerchr14:79161185..79165608hg19UCSC Ensembl
Outerchr14:79157040..79166325hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg389286
hg199286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009704
Samples
Known GenesNRXN3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155036
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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