A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049475



Internal ID19138694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106704732..106869130hg38UCSC Ensembl
Innerchr14:107160749..107277342hg19UCSC Ensembl
Innerchr14:106231794..106348387hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38164399
hg19116594
hg18116594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2161n100
Supporting Variantsnssv3534360
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)nsv1049475
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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