A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054960



Internal ID19144179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104322764..104449190hg38UCSC Ensembl
Innerchr14:104789101..104915527hg19UCSC Ensembl
Innerchr14:103860146..103986572hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38126427
hg19126427
hg18126427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1979n100
Supporting Variantsnssv3711394
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)nsv1054960
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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