A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047429



Internal ID19136648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46684126..46758334hg38UCSC Ensembl
Innerchr14:47153329..47227537hg19UCSC Ensembl
Innerchr14:46223079..46297287hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3874209
hg1974209
hg1874209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1912n100
Supporting Variantsnssv3531674
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)nsv1047429
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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