A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1939n100



Internal ID22788026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74101033..74133932hg38UCSC Ensembl
chr14:74567736..74600635hg19UCSC Ensembl
chr14:73637489..73670388hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3832900
hg1932900
hg1832900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051621, nsv1040006, nsv1045729, nsv1049801, nsv1043877, nsv1037967, nsv1039229, nsv1044674, nsv1051790, nsv1039715, nsv1039710, nsv1035906, nsv1051799, nsv1046204, nsv1050903, nsv1043489
Samples
Known GenesLIN52
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1939n100
Frequency
Sample Size11257
Observed Gain35
Observed Loss0
Observed Complex0
Frequencyn/a


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