A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037214



Internal ID18779745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101506888..101555058hg38UCSC Ensembl
Innerchr14:101973225..102021395hg19UCSC Ensembl
Innerchr14:101042978..101091148hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3848171
hg1948171
hg1848171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1977n100
Supporting Variantsnssv3533555, nssv3533554
Samples
Known GenesDIO3OS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037214
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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