A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3513n100



Internal ID19013881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29978176..30040131hg38UCSC Ensembl
chr19:30469083..30531038hg19UCSC Ensembl
chr19:35160923..35222878hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3861956
hg1961956
hg1861956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057530, nsv1060183, nsv1059975, nsv1063489
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)dgv3513n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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