A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049849



Internal ID19139068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24019175..24044696hg38UCSC Ensembl
Innerchr14:24488384..24513905hg19UCSC Ensembl
Innerchr14:23558224..23583745hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3825522
hg1925522
hg1825522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1850n100
Supporting Variantsnssv3528516
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)nsv1049849
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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