A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040879



Internal ID19130098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38441854..38464870hg38UCSC Ensembl
Innerchr14:38911058..38934074hg19UCSC Ensembl
Innerchr14:37980809..38003825hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3823017
hg1923017
hg1823017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1872n100
Supporting Variantsnssv3528636
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040879
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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