A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1802n100



Internal ID20153418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20881449..20964296hg38UCSC Ensembl
chr14:21349608..21432455hg19UCSC Ensembl
chr14:20419448..20502295hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3882848
hg1982848
hg1882848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051920, nsv1051890, nsv1037218, nsv1043957, nsv1041776, nsv1037668, nsv1043539, nsv1041682, nsv1041549, nsv1054330, nsv1047380, nsv1036896
Samples
Known GenesECRP, RNASE2, RNASE3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1802n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss200
Observed Complex0
Frequencyn/a


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