A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038627



Internal ID18781158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:78169155..78191569hg38UCSC Ensembl
Innerchr14:78635498..78657912hg19UCSC Ensembl
Innerchr14:77705251..77727665hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3822415
hg1922415
hg1822415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531211
Samples
Known GenesNRXN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038627
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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