A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3510n100



Internal ID19013878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29961142..30020645hg38UCSC Ensembl
chr19:30452049..30511552hg19UCSC Ensembl
chr19:35143889..35203392hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3859504
hg1959504
hg1859504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064843, nsv1060537, nsv1067530, nsv1057282, nsv1067099, nsv1060939, nsv1065788, nsv1066223, nsv1064244, nsv1066986, nsv1065923, nsv1055678, nsv1058834
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3510n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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