A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046784



Internal ID19136003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40612245..40756332hg38UCSC Ensembl
Innerchr14:41081450..41225537hg19UCSC Ensembl
Innerchr14:40151200..40295287hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38144088
hg19144088
hg18144088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530150
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)nsv1046784
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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