A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054806



Internal ID19144025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40466959..40741799hg38UCSC Ensembl
Innerchr14:40936163..41211004hg19UCSC Ensembl
Innerchr14:40005913..40280754hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38274841
hg19274842
hg18274842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530146
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)nsv1054806
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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