A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3509n100



Internal ID19013877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29954152..30028098hg38UCSC Ensembl
chr19:30445059..30519005hg19UCSC Ensembl
chr19:35136899..35210845hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3873947
hg1973947
hg1873947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062261, nsv1059959, nsv1063879, nsv1067531, nsv1062880, nsv1063405, nsv1056637
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)dgv3509n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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