A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3430n100



Internal ID19013798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12196893..12267598hg38UCSC Ensembl
chr19:12307708..12378413hg19UCSC Ensembl
chr19:12168708..12239413hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3870706
hg1970706
hg1870706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059883, nsv1059460
Samples
Known GenesLOC100289333
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3430n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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