A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047027



Internal ID19136246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48278315..48384957hg38UCSC Ensembl
Innerchr14:48747518..48854160hg19UCSC Ensembl
Innerchr14:47817268..47923910hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38106643
hg19106643
hg18106643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1917n100
Supporting Variantsnssv3530992
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)nsv1047027
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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