A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1940n100



Internal ID22788027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74104187..74145313hg38UCSC Ensembl
chr14:74570890..74612016hg19UCSC Ensembl
chr14:73640643..73681769hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3841127
hg1941127
hg1841127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052767, nsv1048195
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)dgv1940n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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