A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041332



Internal ID19130551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38464852..38481810hg38UCSC Ensembl
Innerchr14:38934056..38951014hg19UCSC Ensembl
Innerchr14:38003807..38020765hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3816959
hg1916959
hg1816959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528639
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)nsv1041332
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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