A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038839



Internal ID19128058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24018922..24040988hg38UCSC Ensembl
Innerchr14:24488131..24510197hg19UCSC Ensembl
Innerchr14:23557971..23580037hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3822067
hg1922067
hg1822067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1850n100
Supporting Variantsnssv3712261, nssv3528498
Samples
Known GenesDHRS4L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038839
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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