A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054051



Internal ID19143270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:78306271..78338968hg38UCSC Ensembl
Innerchr14:78772614..78805311hg19UCSC Ensembl
Innerchr14:77842367..77875064hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3832698
hg1932698
hg1832698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713531
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)nsv1054051
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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