A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039241



Internal ID19128460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76495274..76657089hg38UCSC Ensembl
Innerchr14:76961617..77123432hg19UCSC Ensembl
Innerchr14:76031370..76193185hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38161816
hg19161816
hg18161816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531208
Samples
Known GenesESRRB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039241
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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