A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1976n100



Internal ID19012344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100937793..101000947hg38UCSC Ensembl
chr14:101404130..101467284hg19UCSC Ensembl
chr14:100473883..100537037hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3863155
hg1963155
hg1863155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036739, nsv1053576, nsv1054883, nsv1044458, nsv1053513, nsv1035568
Samples
Known GenesSNORD113-5, SNORD113-6, SNORD113-7, SNORD113-8, SNORD113-9, SNORD114-1, SNORD114-10, SNORD114-11, SNORD114-12, SNORD114-13, SNORD114-14, SNORD114-15, SNORD114-16, SNORD114-17, SNORD114-18, SNORD114-19, SNORD114-2, SNORD114-20, SNORD114-21, SNORD114-22, SNORD114-23, SNORD114-24, SNORD114-25, SNORD114-26, SNORD114-27, SNORD114-28, SNORD114-29, SNORD114-3, SNORD114-30, SNORD114-31, SNORD114-4, SNORD114-5, SNORD114-6, SNORD114-7, SNORD114-8, SNORD114-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1976n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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