A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054482



Internal ID19143701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104494679..104570679hg38UCSC Ensembl
Innerchr14:104961016..105037016hg19UCSC Ensembl
Innerchr14:104032061..104108061hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3876001
hg1976001
hg1876001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1980n100
Supporting Variantsnssv3533565
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)nsv1054482
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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