A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3511n100



Internal ID19013879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29964373..29988391hg38UCSC Ensembl
chr19:30455280..30479298hg19UCSC Ensembl
chr19:35147120..35171138hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3824019
hg1924019
hg1824019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060763, nsv1061761, nsv1056251, nsv1063717
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)dgv3511n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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