A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528346



Internal ID15455639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:79217613..79280908hg38UCSC Ensembl
Innerchr14:79683956..79747251hg19UCSC Ensembl
Innerchr14:78753709..78817004hg18UCSC Ensembl
Innerchr14:78753709..78817004hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3863296
hg1963296
hg1863296
hg1763296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704930
Samples
Known GenesNRXN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528346
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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