A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046083



Internal ID19135302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46604547..46640857hg38UCSC Ensembl
Innerchr14:47073750..47110060hg19UCSC Ensembl
Innerchr14:46143500..46179810hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3836311
hg1936311
hg1836311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531673
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)nsv1046083
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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