A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046542



Internal ID19135761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24775600..24798002hg38UCSC Ensembl
Innerchr14:25244806..25267208hg19UCSC Ensembl
Innerchr14:24314646..24337048hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3822403
hg1922403
hg1822403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528527
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)nsv1046542
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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