A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049574



Internal ID18792105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106657835..106877229hg38UCSC Ensembl
Innerchr14:107113851..107285437hg19UCSC Ensembl
Innerchr14:106184896..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38219395
hg19171587
hg18171587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2152n100
Supporting Variantsnssv3533062
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)nsv1049574
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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