A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829610



Internal ID16123566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:78690034..78699253hg38UCSC Ensembl
Innerchr14:79156377..79165596hg19UCSC Ensembl
Innerchr14:78226130..78235349hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg389220
hg199220
hg189220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565236
Supporting Variants
Samples
Known GenesNRXN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829610
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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