A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050438



Internal ID19139657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106771605..106877229hg38UCSC Ensembl
Innerchr14:107179847..107285437hg19UCSC Ensembl
Innerchr14:106250892..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38105625
hg19105591
hg18105591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2165n100
Supporting Variantsnssv3534362
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)nsv1050438
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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